CYP21 gene point mutations study in 21-hydroxylase deficiency patients

Zhonghua er ke za zhi. Chinese journal of pediatrics

Volumn 41, Issue 9, 2003, Pages 670-674

  Liao, Xiang yun ^a   Zhang, Ya fen ^a   Gu, Xue fan ^a  

^a XINHUA HOSPITAL AFFILIATED TO SHANGHAI JIAO TONG UNIVERSITY SCHOOL OF MEDICINE   (China)

Author keywords

[No Author keywords available]

Indexed keywords

STEROID 21 MONOOXYGENASE;

ARTICLE; CHILD; CHINA; CONGENITAL ADRENAL HYPERPLASIA; ENZYMOLOGY; FAMILY HEALTH; FEMALE; GENE FREQUENCY; GENETICS; GENOTYPE; HUMAN; INFANT; MALE; METABOLISM; PHENOTYPE; POINT MUTATION; POLYMERASE CHAIN REACTION; PRESCHOOL CHILD; RESTRICTION FRAGMENT LENGTH POLYMORPHISM;

ADRENAL HYPERPLASIA, CONGENITAL; CHILD; CHILD, PRESCHOOL; CHINA; FAMILY HEALTH; FEMALE; GENE FREQUENCY; GENOTYPE; HUMANS; INFANT; MALE; PHENOTYPE; POINT MUTATION; POLYMERASE CHAIN REACTION; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH; STEROID 21-HYDROXYLASE;

EID: 2342473203     PISSN: 05781310     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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