WFS1 in Optic Neuropathies: Mutation Findings in Nonsyndromic Optic Atrophy and Assessment of Clinical Severity-Reference-Cited by-同舟云学术

WFS1 in Optic Neuropathies: Mutation Findings in Nonsyndromic Optic Atrophy and Assessment of Clinical Severity

Published:2016-09 Issue:9 Volume:123 Page:1989-1998
ISSN:0161-6420
Container-title:Ophthalmology
language:en
Short-container-title:Ophthalmology

Author:

Grenier Joanna,Meunier Isabelle^ORCID,Daien Vincent,Baudoin Corinne,Halloy François,Bocquet Béatrice,Blanchet Catherine,Delettre Cécile,Esmenjaud Etienne,Roubertie Agathe,Lenaers Guy,Hamel Christian P.

Publisher

Elsevier BV

Subject

Ophthalmology

Reference39 articles.

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2. Optic atrophy in Wolfram (DIDMOAD) syndrome;Barrett;Eye (Lond),1997

3. Phenotypic characteristics of early Wolfram syndrome;Marshall;Orphanet J Rare Dis,2013

4. A gene encoding a transmembrane protein is mutated in patients with diabetes mellitus and optic atrophy (Wolfram syndrome);Inoue;Nat Genet,1998

5. Two families with nonsyndromic low-frequency hearing loss harbor novel mutations in Wolfram syndrome gene 1;Gürtler;J Mol Med (Berl),2005

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