A novel nonsense mutation in MYO6 is associated with progressive nonsyndromic hearing loss in a Danish DFNA22 family

Kirsten Marie Sanggaard, Klaus Wilbrandt Kjær, H. Eiberg, G. Nurnberg, P. Nurnberg, K. Hoffman, H. Jensen, C. Sorum, Nanna Dahl Rendtorff, L. Tranebjaerg

30 Citationer (Scopus)

Abstract

Udgivelsesdato: 2008/4/15
OriginalsprogEngelsk
TidsskriftAmerican Journal of Medical Genetics. Part A
Vol/bind146A
Udgave nummer8
Sider (fra-til)1017-1025
Antal sider8
ISSN1552-4825
StatusUdgivet - 2008

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