Molecular analysis of the most frequent mutations associated with congenital adrenal hyperplasia secondary to steroid 21-hydroxylase enzyme deficiency;Analisis molecular de las mutaciones mas frecuentes asociadas a la hiperplasia suprarrenal congenita por deficit de la enzima 21 hidroxilasa

Medicina

Volumn 61, Issue 1, 2001, Pages 28-34

  Dardis, Andrea ^a   Marino, Roxana ^a   Bergada, Ignacio ^b   Escobar, Maria Eugenia ^b   Gryngarten, Mirta ^b   Rivarola, Marco A ^a   Belgorosky, Alicia ^a  

^a HOSPITAL DE PEDIATRÍA PROF DR JUAN P GARRAHAN   (Argentina)

^b HOSPITAL DE NIÑOS RICARDO GUTIÉRREZ   (Argentina)

Author keywords

Congenital adrenal hyperplasia; CYP21B gene mutations

Indexed keywords

STEROID 21 MONOOXYGENASE;

ALLELE; ARTICLE; CONGENITAL ADRENAL HYPERPLASIA; FEMALE; GENETICS; HUMAN; MALE; MUTATION; POLYMERASE CHAIN REACTION; SOUTHERN BLOTTING;

ADRENAL HYPERPLASIA, CONGENITAL; ALLELES; BLOTTING, SOUTHERN; FEMALE; HUMANS; MALE; MUTATION; POLYMERASE CHAIN REACTION; STEROID 21-HYDROXYLASE;

EID: 2842575169     PISSN: 00257680     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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