Functional characterisation of a natural androgen receptor missense mutation (N771H) causing human androgen insensitivity syndrome
Author:
Publisher
Wiley
Subject
Urology,Endocrinology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1439-0272.2011.01219.x/fullpdf
Reference20 articles.
1. Partial androgen insensitivity caused by an androgen receptor mutation at amino acid 907 (gly - arg) that results in decreased ligand binding affinity and reduced androgen receptor messenger ribonucleic acid levels;Choong;J Clin Endocrinol Metab,1996
2. Androgen receptor structural and functional elements: role and regulation in prostate cancer;Dehm;Mol Endocrinol,2007
3. Anatomy of the steroid receptor zinc finger region;Freedman;Endocr Rev,1992
4. Detection of point mutations in the androgen receptor gene using non- isotopic single strand conformation polymorphism analysis. German Collaborative Intersex Study Group;Hiort;Hum Mol Genet,1994
5. The clinical and molecular spectrum of androgen insensitivity syndromes;Hiort;Am J Med Genet,1996
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