Mutational analysis of androgen receptor gene in two families with androgen insensitivity

Background: Androgen insensitivity syndrome (AIS) is a rare X-linked disorder due to mutations in the androgen receptor (AR) gene causing end-organ resistance to the androgenic hormone. Subjects and Methods: Genetic studies were carried out in two families by karyotype and targeted exome sequencing...

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Auteur principal:	Radha Ramadevi Akella
Format:	Artigo
Langue:	Inglês
Publié:	Wolters Kluwer Medknow Publications 2017-01-01
Collection:	Indian Journal of Endocrinology and Metabolism
Sujets:	Androgen insensitivity syndrome androgen receptor gene mutation X-linked recessive disorder XY karyotype
Accès en ligne:	http://www.ijem.in/article.asp?issn=2230-8210;year=2017;volume=21;issue=4;spage=520;epage=523;aulast=Akella
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