A novel arg616Cys mutation in the DNA-binding domain of complete androgen insensitivity syndrome in

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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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