Mutational spectrum of theWFS1 gene in Wolfram syndrome, nonsyndromic hearing impairment, diabetes mellitus, and psychiatric disease-Reference-Cited by-同舟云学术

Mutational spectrum of theWFS1 gene in Wolfram syndrome, nonsyndromic hearing impairment, diabetes mellitus, and psychiatric disease

Published:2003-08-29 Issue:4 Volume:22 Page:275-287
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Cryns Kim,Sivakumaran Theru A.,Van den Ouweland Jody M.W.,Pennings Ronald J.E.,Cremers Cor W.R.J.,Flothmann Kris,Young Terry-Lynn,Smith Richard J.H.,Lesperance Marci M.,Camp Guy Van

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference57 articles.

1. Missense Variations of the Gene Responsible for Wolfram Syndrome (WFS1/wolframin) in Japanese: Possible Contribution of the Arg456His Mutation to Type 1 Diabetes as a Nonautoimmune Genetic Basis

2. Neurodegeneration and diabetes: UK nationwide study of Wolfram (DIDMOAD) syndrome

3. A nuclear defect in the 4p16 region predisposes to multiple mitochondrial DNA deletions in families with Wolfram syndrome.

4. Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss

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