Connexin 26 mutation in keratitis-ichthyosis-deafness (KID) syndrome in mother and daughter with combined conductive and sensorineural hearing loss

Brent Kelly, Annabelle Lozano, Guillermo Altenberg, Tomoko Makishima

Research output: Contribution to journal › Article › peer-review

13 Scopus citations

Fingerprint

Dive into the research topics of 'Connexin 26 mutation in keratitis-ichthyosis-deafness (KID) syndrome in mother and daughter with combined conductive and sensorineural hearing loss'. Together they form a unique fingerprint.

Pharmacology, Toxicology and Pharmaceutical Science

INIS

Neuroscience

Biochemistry, Genetics and Molecular Biology

Keyphrases