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PMID 25677139
Gene Name AR
Condition Azoospermia
Association In summary, an insertion mutation together with a known point variation was described in the TAD of AR gene. They could be responsible for the impaired spermatogenesis, and this research would enrich the AR database and extend the current understanding of
Mutation g. 1283_1284insAGTTTGCTG, insertion of three proteins (serine-leucine-leucine) between codon 56 and codon 57, p.Gln58Leu substitution
Population size 1
Population details 1
Age 25yrs
Sex Male
Infertility type Male infertility
Other associated phenotypes Azoospermia


An insertion mutation in the androgen receptor gene in a patient with azoospermia

Chen YH, Xu HY, Wang ZY, Zhu ZH, Li CD, Wu ZG, Chen BC.

No abstract available