Mutations of the phenylalanine hydroxylase gene in patients with phenylketonuria in Shanxi, China

Genetics and Molecular Biology

Volumn 35, Issue 4, 2012, Pages 709-713

  Zhou, Yong An ^a   Ma, Yun Xia ^a   Zhang, Quan Bin ^a   Gao, Wei Hua ^b   Liu, Jian Ping ^c   Yang, Jian Ping ^c   Zhang, Gai Xiu ^c   Zhang, Xiao Gang ^c   Yu, Liang ^c  

^a Taiyuan City Centre Hospital   (China)

^b SHANXI MEDICAL UNIVERSITY   (China)

^c Shanxi Modern Women Hospital   (China)

Author keywords

Gene mutation; Phenylalanine hydroxylase; Phenylketonuria

Indexed keywords

COMPLEMENTARY DNA;

ARTICLE; CHILD; CHINA; CODON; CONTROLLED STUDY; EXON; FEMALE; GENE; GENE DELETION; GENE FREQUENCY; GENE LOCUS; HETEROZYGOSITY LOSS; HUMAN; INCIDENCE; INFANT; MAJOR CLINICAL STUDY; MALE; MISSENSE MUTATION; MUTATIONAL ANALYSIS; PATHOGENESIS; PHENYLALANINE HYDROXYLASE GENE; PHENYLKETONURIA; PRESCHOOL CHILD; SCHOOL CHILD; SEQUENCE ALIGNMENT; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 84871606053     PISSN: 14154757     EISSN: 16784685     Source Type: Journal    
DOI: 10.1590/S1415-47572012005000069     Document Type: Article

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