Clinical and molecular characteristics in 15 patients with androgen receptor gene mutations from South China

Author:

Su L.1,Cheng J.1,Yin X.1,Liu G.2,Lu Z.1,Sheng H.1,Cai Y.1,Shi Q.3,Liu L.1

Affiliation:

1. Department of Genetics and Endocrinology; Guangzhou Women and Children's Medical Center; Guangzhou Medical University; Guangzhou Guangdong China

2. Department of Pediatric Urology; Guangzhou Women and Children's Medical Center; Guangzhou Medical University; Guangzhou Guangdong China

3. Department of Pathology; Guangzhou Women and Children's Medical Center; Guangzhou Medical University; Guangzhou Guangdong China

Funder

National “Twelfth Five-Year” Plan for Science and Technology, China

Publisher

Wiley

Subject

Urology,Endocrinology,General Medicine

Reference32 articles.

1. Novel (60%) and recurrent (40%) androgen receptor gene mutations in a series of 59 patients with a 46, XY disorder of sex development;Audi;The Journal of Clinical Endocrinology and Metabolism,2010

2. Complete androgen insensitivity syndrome associated with male gender identity or female precocious puberty in the same family;Bermudez de la Vega;Sexual Development: Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation,2015

3. Isolated micropenis reveals partial androgen insensitivity syndrome confirmed by molecular analysis;Bhangoo;Asian Journal of Andrology,2010

4. Androgen receptor gene mutation, rearrangement, polymorphism;Eisermann;Translational Andrology and Urology,2013

5. Male infertility and androgen receptor gene mutations: Clinical features and identification of seven novel mutations;Ferlin;Clinical Endocrinology,2006

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