换一批
换一批A novel arg616Cys mutation in the DNA-binding domain of complete androgen insensitivity syndrome in a Chinese family
摘要Awide spectrum of Androgen insensitivity syndrome (AIS) occur due to mutations in the androgen receptor (AR).The clinical presentation of AIS ranges from a typically male phenotype with decreased body hair and/or oligospermia to a typically female phenotype with primary amenorrhea and without pubic and axillary hair;the latter phenotype is categorized as complete AIS (CAIS).
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栏目名称
DOI
10.3760/cma.j.issn.0366-6999.20123249
发布时间
2013-12-06
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