Associated Papers
WS1 gene mutation analysis of Wolfram syndrome in a Chinese patient and a systematic review of literatures.
Yu G et al.
Endocrine, 2010
Mutational spectrum of the WFS1 gene in Wolfram syndrome, nonsyndromic hearing impairment, diabetes mellitus, and psychiatric disease.
Cryns K et al.
Human Mutation, 2003
Molecular characterization of WFS1 in patients with Wolfram syndrome.
van ven Ouweland JM et al.
The Journal of Molecular Diagnostics : Jmd, 2003
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