Article
Prevalence and phenotypic features of diabetes due to recessive, non-syndromic WFS1 mutations.
European journal of endocrinology - 10 Dec 2021
Zhu Mingqiang, Li Yangxi, Dong Guanping, Chen Xuefeng, Huang Ke, Wu Wei, Dai Yangli, Zhang Li, Lin Hu, Wang Sihua, Polychronakos Constantin, Fu Junfen
Abstract excerpt
OBJECTIVE: Recessive WFS1 mutations are known to cause Wolfram syndrome, a very rare systemic disorder. However, they were also found in non-syndromic diabetes in Han Chinese misdiagnosed with type 1 diabetes (T1D), a molecular cause that appears to be considerably more common than the fully expressed syndrome. We aimed to better define the incidence and clinical features of non-syndromic diabetes due to...
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