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Homozygous DMRT1 mutation c.967G>A found in a Chinese patient with 46,XY complete gonadal dysgenesis and review of literature

2021-03-29

Abstract excerpt

A Chinese woman with 46,XY CGD was diagnosed by clinicopathologic findings . A homozygous mutation c.967G>A(p. Val323Ile) in the DMRT1 gene was detected in the patient by WES. As far as we know, this is the first case of 46,XY CGD caused by a homozygous mutation in the DMRT1 gene.

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Identifiers and source

Literature Corpus work
f3ac47c6-56dc-5ffd-9b6b-788ed9196772
DOI
10.22541/au.161699356.65959936/v1
Open publication

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