The Precise Diagnosis of Wolfram Syndrome Type 1 Based on Next-Generation Sequencing

Author:

Wang Dan-Dan,Hu Fang-Yuan,Gao Feng-Juan,Zhang Sheng-Hai,Xu Ping,Tian Guo-Hong,Wu Ji-Hong

Funder

National Natural Science Foundation of China

Publisher

Frontiers Media SA

Subject

Genetics(clinical),Genetics,Molecular Medicine

Reference49 articles.

1. Wolfram syndrome: new mutations, different phenotype;Aloi;PLoS ONE,2012

2. A new mutation in WFS1 gene (C.1522-1523delTA, Y508fsX421) may be responsible for early appearance of clinical features of wolfram syndrome and suicidal behaviour;Aluclu;Neuro Endocrinol. Lett,2006

3. Neurodegeneration and diabetes: UK nationwide study of Wolfram (DIDMOAD) syndrome;Barrett;Lancet,1995

4. A case of Wolfram syndrome with anosmia and neurogenic bladder;Chai;Jiangsu Med. J.,2003

5. Wolfram syndrome (diabetes insipidus, diabetes, optic atrophy, and deafness): clinical and genetic study;D'Annunzio;Diabetes Care,2008

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