共 50 条
- [41] A novel variant of the WFS1 gene with dominant inheritance causing Wolfram-like syndrome HORMONE RESEARCH IN PAEDIATRICS, 2019, 91 : 401 - 401
- [46] Unique three-site compound heterozygous mutation in the WFS1 gene in Wolfram syndrome BMC Endocrine Disorders, 21
- [47] Function of WFS1 and WFS2 in the Central Nervous System: Implications for Wolfram Syndrome and Alzheimer's disease NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS, 2020, 118 : 775 - 783
- [49] c.2425G>A mutation in the WFS1 gene associated with Wolfram syndrome: a case report International Journal of Diabetes in Developing Countries, 2019, 39 : 232 - 235