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 Citations (Scopus)

Abstract

Udgivelsesdato: 2006/5
Original languageEnglish
JournalJournal of Medical Genetics
Volume43
Issue number5
Pages (from-to)435-440
Number of pages5
ISSN1468-6244
Publication statusPublished - 2006

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