Autosomal dominant optic atrophy associated with hearing impairment and impaired glucose regulation caused by a missense mutation in the WFS1 gene

Hans Rudolf Lytchoff Eiberg, Lars Hansen, B. Kjer, T. Hansen, O. Pedersen, M. Bille, T. Rosenberg, L. Tranebjaerg

79 Citationer (Scopus)

Abstract

Udgivelsesdato: 2006/5
OriginalsprogEngelsk
TidsskriftJournal of Medical Genetics
Vol/bind43
Udgave nummer5
Sider (fra-til)435-440
Antal sider5
ISSN1468-6244
StatusUdgivet - 2006

Citationsformater