Spectrum of phenylalanine hydroxylase gene mutations and genotype-phenotype correlation in the patients with phenylketonuria in Beijing area of China.

Zhonghua er ke za zhi. Chinese journal of pediatrics

Volumn 46, Issue 2, 2008, Pages 115-119

  Qu, Yu jin ^a   Song, Fang ^b   Jin, Yu wei ^b   Wang, Hong ^b   Zhang, Yu min ^b   Qin, Jin li ^b   Qiu, Lei ^b  

^a CAPITAL INSTITUTE OF PEDIATRICS   (China)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

PHENYLALANINE 4 MONOOXYGENASE;

ALLELE; ARTICLE; CHINA; GENETIC ASSOCIATION; GENETIC POLYMORPHISM; GENETICS; GENOTYPE; HUMAN; INTRON; MUTATION; NEWBORN; PHENOTYPE; PHENYLKETONURIA;

ALLELES; CHINA; GENETIC ASSOCIATION STUDIES; GENOTYPE; HUMANS; INFANT, NEWBORN; INTRONS; MUTATION; PHENOTYPE; PHENYLALANINE HYDROXYLASE; PHENYLKETONURIAS; POLYMORPHISM, GENETIC;

EID: 76749109171     PISSN: 05781310     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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