Two novel glucose 6-phosphate dehydrogenase deficiency mutations and association of such mutations with F8C/G6PD haplotype in Chinese

Journal of the Formosan Medical Association

Volumn 96, Issue 12, 1997, Pages 948-954

  Chen, Hua Ling ^a   Huang, May Jen ^b   Huang, Ching Shan ^b   Tang, Tang K ^a,c  

^a NATIONAL TAIWAN UNIVERSITY   (Taiwan)

^b CATHAY GENERAL HOSPITAL   (Taiwan)

^c INSTITUTE OF BIOMEDICAL SCIENCES   (Taiwan)

Author keywords

Chinese; Coagulation factor VIII; Glucose 6 phosphate dehydrogenase deficiency; Haplotype; Polymorphism

Indexed keywords

ARTICLE; CHINESE; FEMALE; GENE LINKAGE DISEQUILIBRIUM; GENE MUTATION; GENETIC ASSOCIATION; GENETIC POLYMORPHISM; GLUCOSE 6 PHOSPHATE DEHYDROGENASE DEFICIENCY; HAPLOTYPE; HUMAN; MAJOR CLINICAL STUDY; MALE; NEWBORN; NUCLEIC ACID BASE SUBSTITUTION; POLYMERASE CHAIN REACTION; SINGLE STRAND CONFORMATION POLYMORPHISM;

FEMALE; GLUCOSEPHOSPHATE DEHYDROGENASE; GLUCOSEPHOSPHATE DEHYDROGENASE DEFICIENCY; HAPLOTYPES; HUMANS; MALE; MUTATION;

EID: 0031417640     PISSN: 09296646     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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