共 50 条
- [23] Wolfram syndrome: Phenotypic heterogeneity and novel genetic variants in the WFS1 gene ENDOCRINOLOGIA DIABETES Y NUTRICION, 2022, 69 (02): : 153 - 154
- [24] Clinical Characteristics of Wolfram Syndrome in Chinese Population and a Novel Frameshift Mutation in WFS1 FRONTIERS IN ENDOCRINOLOGY, 2018, 9
- [25] Identification of a novel WFS1 homozygous nonsense mutation in Jordanian children with Wolfram syndrome META GENE, 2016, 9 : 219 - 224
- [26] Mutation analysis of the WFS1 gene in a Chinese family with autosomal-dominant non-syndrome deafness SCIENTIFIC REPORTS, 2022, 12 (01):
- [27] Effect of 4-phenylbutyrate and valproate on dominant mutations of WFS1 gene in Wolfram syndrome Journal of Endocrinological Investigation, 2020, 43 : 1317 - 1325