Erratum: De novo missense variants in exon 9 of SEPHS1 cause a neurodevelopmental condition with developmental delay, poor growth, hypotonia, and dysmorphic features (The American Journal of Human Genetics (2024) 111(4) (778–790), (S0002929724000739), (10.1016/j.ajhg.2024.02.016))

Care4Rare Canada Consortium; Undiagnosed Diseases Network

doi:10.1016/j.ajhg.2024.05.004

Erratum: De novo missense variants in exon 9 of SEPHS1 cause a neurodevelopmental condition with developmental delay, poor growth, hypotonia, and dysmorphic features (The American Journal of Human Genetics (2024) 111(4) (778–790), (S0002929724000739), (10.1016/j.ajhg.2024.02.016))

Care4Rare Canada Consortium, Undiagnosed Diseases Network

Internal Medicine

Research output: Contribution to journal › Comment/debate › peer-review

Abstract

(The American Journal of Human Genetics 111, 778–790; April 4, 2024) In the originally published version of the paper, the placement of the final two authors was incorrect. Both Jane Juusola and Jun Yang are co-senior authors; J.J. should appear second-to-last and J.Y. appear last. The authors apologize for this error.

Original language	English (US)
Pages (from-to)	1240
Number of pages	1
Journal	American Journal of Human Genetics
Volume	111
Issue number	6
DOIs	https://doi.org/10.1016/j.ajhg.2024.05.004
State	Published - Jun 6 2024

ASJC Scopus subject areas

Genetics
Genetics(clinical)

Access to Document

10.1016/j.ajhg.2024.05.004

Fingerprint

Dive into the research topics of 'Erratum: De novo missense variants in exon 9 of SEPHS1 cause a neurodevelopmental condition with developmental delay, poor growth, hypotonia, and dysmorphic features (The American Journal of Human Genetics (2024) 111(4) (778–790), (S0002929724000739), (10.1016/j.ajhg.2024.02.016))'. Together they form a unique fingerprint.

Cite this

Care4Rare Canada Consortium, & Undiagnosed Diseases Network (2024). Erratum: De novo missense variants in exon 9 of SEPHS1 cause a neurodevelopmental condition with developmental delay, poor growth, hypotonia, and dysmorphic features (The American Journal of Human Genetics (2024) 111(4) (778–790), (S0002929724000739), (10.1016/j.ajhg.2024.02.016)). American Journal of Human Genetics, 111(6), 1240. https://doi.org/10.1016/j.ajhg.2024.05.004

Erratum: De novo missense variants in exon 9 of SEPHS1 cause a neurodevelopmental condition with developmental delay, poor growth, hypotonia, and dysmorphic features (The American Journal of Human Genetics (2024) 111(4) (778–790), (S0002929724000739), (10.1016/j.ajhg.2024.02.016)). / Care4Rare Canada Consortium; Undiagnosed Diseases Network.
In: American Journal of Human Genetics, Vol. 111, No. 6, 06.06.2024, p. 1240.

Research output: Contribution to journal › Comment/debate › peer-review

Care4Rare Canada Consortium & Undiagnosed Diseases Network 2024, 'Erratum: De novo missense variants in exon 9 of SEPHS1 cause a neurodevelopmental condition with developmental delay, poor growth, hypotonia, and dysmorphic features (The American Journal of Human Genetics (2024) 111(4) (778–790), (S0002929724000739), (10.1016/j.ajhg.2024.02.016))', American Journal of Human Genetics, vol. 111, no. 6, pp. 1240. https://doi.org/10.1016/j.ajhg.2024.05.004

Care4Rare Canada Consortium, Undiagnosed Diseases Network. Erratum: De novo missense variants in exon 9 of SEPHS1 cause a neurodevelopmental condition with developmental delay, poor growth, hypotonia, and dysmorphic features (The American Journal of Human Genetics (2024) 111(4) (778–790), (S0002929724000739), (10.1016/j.ajhg.2024.02.016)). American Journal of Human Genetics. 2024 Jun 6;111(6):1240. doi: 10.1016/j.ajhg.2024.05.004

Care4Rare Canada Consortium ; Undiagnosed Diseases Network. / Erratum : De novo missense variants in exon 9 of SEPHS1 cause a neurodevelopmental condition with developmental delay, poor growth, hypotonia, and dysmorphic features (The American Journal of Human Genetics (2024) 111(4) (778–790), (S0002929724000739), (10.1016/j.ajhg.2024.02.016)). In: American Journal of Human Genetics. 2024 ; Vol. 111, No. 6. pp. 1240.

@article{ebfa2f64765c4d2ba3cde711d8f82cbd,

title = "Erratum: De novo missense variants in exon 9 of SEPHS1 cause a neurodevelopmental condition with developmental delay, poor growth, hypotonia, and dysmorphic features (The American Journal of Human Genetics (2024) 111(4) (778–790), (S0002929724000739), (10.1016/j.ajhg.2024.02.016))",

abstract = "(The American Journal of Human Genetics 111, 778–790; April 4, 2024) In the originally published version of the paper, the placement of the final two authors was incorrect. Both Jane Juusola and Jun Yang are co-senior authors; J.J. should appear second-to-last and J.Y. appear last. The authors apologize for this error.",

author = "{Care4Rare Canada Consortium} and {Undiagnosed Diseases Network} and Mullegama, {Sureni V.} and Kiernan, {Kaitlyn A.} and Erin Torti and Ethan Pavlovsky and Nicholas Tilton and Austin Sekula and Hua Gao and Alaimo, {Joseph T.} and Kendra Engleman and Rush, {Eric T.} and Karli Blocker and Dipple, {Katrina M.} and Fettig, {Veronica M.} and Heather Hare and Ian Glass and Grange, {Dorothy K.} and Michael Griffin and Chanika Phornphutkul and Lauren Massingham and Lakshmi Mehta and Miller, {Danny E.} and Jenny Thies and Merritt, {J. Lawrence} and Eric Muller and Matthew Osmond and Sawyer, {Sarah L.} and Rachel Slaugh and Hickey, {Rachel E.} and Barry Wolf and Sanjeev Choudhary and Miljan Simonovi{\'c} and Yueqing Zhang and Palculict, {Timothy Blake} and Aida Telegrafi and Carere, {Deanna Alexis} and Wentzensen, {Ingrid M.} and Morrow, {Michelle M.} and Monaghan, {Kristin G.} and Jane Juusola and Jun Yang",

note = "Publisher Copyright: {\textcopyright} 2024 American Society of Human Genetics",

year = "2024",

month = jun,

day = "6",

doi = "10.1016/j.ajhg.2024.05.004",

language = "English (US)",

volume = "111",

pages = "1240",

journal = "American Journal of Human Genetics",

issn = "0002-9297",

publisher = "Cell Press",

number = "6",

}

TY - JOUR

T1 - Erratum

T2 - De novo missense variants in exon 9 of SEPHS1 cause a neurodevelopmental condition with developmental delay, poor growth, hypotonia, and dysmorphic features (The American Journal of Human Genetics (2024) 111(4) (778–790), (S0002929724000739), (10.1016/j.ajhg.2024.02.016))

AU - Care4Rare Canada Consortium

AU - Undiagnosed Diseases Network

AU - Mullegama, Sureni V.

AU - Kiernan, Kaitlyn A.

AU - Torti, Erin

AU - Pavlovsky, Ethan

AU - Tilton, Nicholas

AU - Sekula, Austin

AU - Gao, Hua

AU - Alaimo, Joseph T.

AU - Engleman, Kendra

AU - Rush, Eric T.

AU - Blocker, Karli

AU - Dipple, Katrina M.

AU - Fettig, Veronica M.

AU - Hare, Heather

AU - Glass, Ian

AU - Grange, Dorothy K.

AU - Griffin, Michael

AU - Phornphutkul, Chanika

AU - Massingham, Lauren

AU - Mehta, Lakshmi

AU - Miller, Danny E.

AU - Thies, Jenny

AU - Merritt, J. Lawrence

AU - Muller, Eric

AU - Osmond, Matthew

AU - Sawyer, Sarah L.

AU - Slaugh, Rachel

AU - Hickey, Rachel E.

AU - Wolf, Barry

AU - Choudhary, Sanjeev

AU - Simonović, Miljan

AU - Zhang, Yueqing

AU - Palculict, Timothy Blake

AU - Telegrafi, Aida

AU - Carere, Deanna Alexis

AU - Wentzensen, Ingrid M.

AU - Morrow, Michelle M.

AU - Monaghan, Kristin G.

AU - Juusola, Jane

AU - Yang, Jun

PY - 2024/6/6

Y1 - 2024/6/6

N2 - (The American Journal of Human Genetics 111, 778–790; April 4, 2024) In the originally published version of the paper, the placement of the final two authors was incorrect. Both Jane Juusola and Jun Yang are co-senior authors; J.J. should appear second-to-last and J.Y. appear last. The authors apologize for this error.

AB - (The American Journal of Human Genetics 111, 778–790; April 4, 2024) In the originally published version of the paper, the placement of the final two authors was incorrect. Both Jane Juusola and Jun Yang are co-senior authors; J.J. should appear second-to-last and J.Y. appear last. The authors apologize for this error.

UR - http://www.scopus.com/inward/record.url?scp=85192948793&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=85192948793&partnerID=8YFLogxK

U2 - 10.1016/j.ajhg.2024.05.004

DO - 10.1016/j.ajhg.2024.05.004

M3 - Comment/debate

C2 - 38749428

AN - SCOPUS:85192948793

SN - 0002-9297

VL - 111

SP - 1240

JO - American Journal of Human Genetics

JF - American Journal of Human Genetics

IS - 6

ER -

Erratum: De novo missense variants in exon 9 of SEPHS1 cause a neurodevelopmental condition with developmental delay, poor growth, hypotonia, and dysmorphic features (The American Journal of Human Genetics (2024) 111(4) (778–790), (S0002929724000739), (10.1016/j.ajhg.2024.02.016))

Abstract

ASJC Scopus subject areas

Access to Document

Other files and links

Fingerprint

Cite this