G6PD nankang (517 T→C; 173 Phe→Leu): A new chinese g6pd variant associated with neonatal jaundice

Human Heredity

Volumn 46, Issue 4, 1996, Pages 201-204

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

^a INSTITUTE OF BIOMEDICAL SCIENCES   (Taiwan)

^b NATIONAL TAIWAN UNIVERSITY   (Taiwan)

^c CATHAY GENERAL HOSPITAL   (Taiwan)

Author keywords

Chinese; F8C G6PD haplotype; Glucose 6 phosphate dehydrogenase deficiency; Mutation; Neonatal jaundice

Indexed keywords

ENZYME VARIANT; GLUCOSE 6 PHOSPHATE DEHYDROGENASE;

ALLELE; AMINO ACID SUBSTITUTION; ARTICLE; CASE REPORT; CHINESE; GENE MUTATION; HUMAN; HUMAN CELL; MALE; NEWBORN JAUNDICE; POINT MUTATION; POLYMERASE CHAIN REACTION; RESTRICTION SITE; SINGLE STRAND CONFORMATION POLYMORPHISM;

FETAL BLOOD; GLUCOSEPHOSPHATE DEHYDROGENASE; GLUCOSEPHOSPHATE DEHYDROGENASE DEFICIENCY; HAPLOTYPES; HUMANS; INFANT, NEWBORN; JAUNDICE, NEONATAL; MALE; POINT MUTATION; POLYMERASE CHAIN REACTION; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; VARIATION (GENETICS);

EID: 0029884274     PISSN: 00015652     EISSN: 14230062     Source Type: Journal    
DOI: 10.1159/000154354     Document Type: Article

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