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A new point mutation of the androgen receptor gene in a patient with partial androgen resistance and severe oligozoospermia.
Knoke, I; Jakubiczka, S; Lehnert, H; Wieacker, P.
Affiliation
  • Knoke I; Institut für Humangenetik, Universitätsklinikum Magdeburg, Germany.
Andrologia ; 31(4): 199-201, 1999 Jul.
Article in En | MEDLINE | ID: mdl-10470409
Mutations of the androgen receptor gene in genetic males cause a variety of androgen insensitivity syndromes varying from female phenotype through intersexuality to male phenotype with infertility. The identification of a missense mutation in the steroid-binding domain in an infertile male with mild features of androgen insensitivity is reported here.
Subject(s)
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Collection: 01-internacional Database: MEDLINE Main subject: Oligospermia / Androgen-Insensitivity Syndrome / Receptors, Androgen / Point Mutation Type of study: Prognostic_studies Limits: Adult / Female / Humans / Male Language: En Journal: Andrologia Year: 1999 Document type: Article Affiliation country: Germany Country of publication: Germany
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Collection: 01-internacional Database: MEDLINE Main subject: Oligospermia / Androgen-Insensitivity Syndrome / Receptors, Androgen / Point Mutation Type of study: Prognostic_studies Limits: Adult / Female / Humans / Male Language: En Journal: Andrologia Year: 1999 Document type: Article Affiliation country: Germany Country of publication: Germany