Literature DB >> 25404833

A case of complete androgen insensitivity syndrome: genetic analysis of the family.

Sunil K Kota1, Gayatri Kotni2, Jaya P Pani3, Kirtikumar D Modi1.   

Abstract

Year:  2013        PMID： 25404833      PMCID： PMC4228012          DOI： 10.1007/s13224-013-0400-8

Source DB:  PubMed          Journal:  J Obstet Gynaecol India        ISSN： 0975-6434


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  3 in total

1.  Androgen-insensitivity syndrome as a possible coactivator disease.

Authors:  M Adachi; R Takayanagi; A Tomura; K Imasaki; S Kato; K Goto; T Yanase; S Ikuyama; H Nawata
Journal:  N Engl J Med       Date:  2000-09-21       Impact factor: 91.245

2.  A novel c.C2754 > T transition in the androgen receptor gene introduces the premature termination codon Q798X and results in a truncated form of the receptor.

Authors:  M Ignacak; J Turek-Plewa; J Limon; W H Trzeciak
Journal:  Gynecol Endocrinol       Date:  2004-10       Impact factor: 2.260

3.  The androgen receptor gene mutations database (ARDB): 2004 update.

Authors:  Bruce Gottlieb; Lenore K Beitel; Jian Hui Wu; Mark Trifiro
Journal:  Hum Mutat       Date:  2004-06       Impact factor: 4.878
  3 in total

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