Vestibular Dysfunction in DFNB1 deafness

Mutations of GJB2 and GJB6 (connexin-26 and 30) at the DFNB1 locus are the most common cause of autosomal recessive, nonsyndromic deafness. Despite their widespread expression throughout the vestibular system, vestibular dysfunction has not been widely recognized as a commonly associated clinical fe...

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Bibliografski detalji
Glavni autori: Dodson, Kelley M, Blanton, Susan H, Welch, Katherine O, Norris, Virginia W, Nuzzo, Regina L, Wegelin, Jacob A., Marin, Ruth S, Nance, Walter E, Pandya, Arti, Arnos, Kathleen S
Format: Artigo
Jezik:Inglês
Izdano: 2011
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Article
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3080433/
https://ncbi.nlm.nih.gov/pubmed/21465647
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.a.33828
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