Atypical familial diabetes associated with a novel NEUROD1 nonsense variant

Journal of Pediatric Endocrinology and Metabolism(2022)

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摘要
Abstract Objectives We aimed to identify the origin of atypical diabetes in a family with four generations of diabetes from South Asia. The family members showed different clinical phenotypes. Members of generation one to three were presumed to have type 2 diabetes and generation four to have type 1 diabetes. Case presentation We performed a genetic analysis of the family using targeted high throughput sequencing. Conclusions We identified a novel nonsense variant in the neurogenic differentiation 1 (NEUROD1) gene, co-segregating with diabetes. The variant was located in the DNA-binding domain, altering a protein residue that was very well conserved among different species.
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关键词
high throughput sequencing,MODY,monogenic diabetes
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