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PMID 8103398
Gene Name AR
Condition CAIS
Association An exonic point mutation creates a MaeIII site in the androgen receptor gene of a family with completeandrogen insensitivity syndrome.
Sex Male, Female
Infertility type Male infertility, Female infertility
Other associated phenotypes CAIS


An exonic point mutation creates a MaeIII site in the androgen receptor gene of a family with complete androgen insensitivity syndrome

Lobaccaro JM, Lumbroso S, Ktari R, Dumas R, Sultan C.

No abstract available