Associated Papers
Mutation of c.244G>T in NR5A1 gene causing 46, XY DSD by affecting RNA splicing.
Yu B et al.
Orphanet Journal of Rare Diseases, 2021
[Clinical and molecular characteristics of patients with 46,XY DSD due to NR5A1 gene mutations].
Kalinchenko NY et al.
Problemy Endokrinologii, 2020
Prevalence of gene mutations in a Chinese 46,XY disorders of sex development cohort detected by targeted next-generation sequencing.
Yu BQ et al.
Asian Journal of Andrology, 0
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