A new missense substitution at a mutational hot spot of the androgen receptor in siblings with complete androgen insensitivity syndrome.

Human mutation

Volumn 11, Issue 4, 1998, Pages 337-339

  Dork T ^a   Schnieders, F ^a   Jakubiczka, S ^a   Wieacker, P ^a   Schroeder Kurth, T ^a   Schmidtke, J ^a  

^a HANNOVER MEDICAL SCHOOL   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ANDROGEN RECEPTOR;

ADULT; ANDROGEN INSENSITIVITY SYNDROME; ARTICLE; CASE REPORT; EXON; GENETICS; HUMAN; KARYOTYPING; MALE; PATHOPHYSIOLOGY; PHENOTYPE; PHYSIOLOGY; POINT MUTATION; PRENATAL DEVELOPMENT; SEX DIFFERENTIATION;

ADULT; ANDROGEN-INSENSITIVITY SYNDROME; EXONS; HUMANS; KARYOTYPING; MALE; PHENOTYPE; POINT MUTATION; RECEPTORS, ANDROGEN; SEX DIFFERENTIATION;

EID: 0031638548     PISSN: 10597794     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (0)