Characterization of a novel receptor mutation A-->T at exon 4 in complete androgen insensitivity syndrome and a carrier sibling via bidirectional polymorphism sequence analysis.

International journal of molecular medicine

Volumn 9, Issue 1, 2002, Pages 45-48

  Sills, E Scott ^a   Sholes, Thomas E ^a   Perloe, Mark ^a   Kaplan, Carolyn R ^a   Davis, Jessica G ^a   Tucker, Michael J ^a  

^a Georgia Reproductive Specialists LLC   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANDROGEN RECEPTOR;

ADULT; ANDROGEN INSENSITIVITY SYNDROME; ARTICLE; CASE REPORT; DNA SEQUENCE; EXON; FEMALE; GENETIC POLYMORPHISM; GENETICS; HETEROZYGOTE; HUMAN; MALE; POINT MUTATION;

ADULT; ANDROGEN-INSENSITIVITY SYNDROME; EXONS; FEMALE; HETEROZYGOTE; HUMANS; MALE; POINT MUTATION; POLYMORPHISM, GENETIC; RECEPTORS, ANDROGEN; SEQUENCE ANALYSIS, DNA;

MLCS; MLOWN;

EID: 0036134167     PISSN: 11073756     EISSN: None     Source Type: Journal    
DOI: 10.3892/ijmm.9.1.45     Document Type: Article

References (0)