Identification of the Underlying Androgen Receptor Defect in the Dallas Reifenstein Family

CONTEXT: The Dallas Reifenstein family — first described in 1965 — includes 14 known members with partial androgen insensitivity syndrome (PAIS). However, the underlying molecular defect was never identified. OBJECTIVE: To identify the underlying genetic defect for PAIS in the Dallas Reifenstein fam...

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Detalles Bibliográficos
Autores principales: Ahmad, Zahid, Xing, Chao, Panach, Kamaldeep, Kittler, Ralf, McPhaul, Michael J., Wilson, Jean D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Endocrine Society 2017
Materias:
Clinical Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5686667/
https://www.ncbi.nlm.nih.gov/pubmed/29264534
http://dx.doi.org/10.1210/js.2017-00124

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5686667/
https://www.ncbi.nlm.nih.gov/pubmed/29264534
http://dx.doi.org/10.1210/js.2017-00124

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