Molecular characterization of glucose-6-phosphate dehydrogenase deficiency in the Han and Li nationalities in Hainan, China and identification of a new mutation in human G6PD gene

Chinese Journal of Medical Genetics

Volumn 18, Issue 2, 2001, Pages 105-109

  Wangwei, C ^a   Filosa, S ^a   Martini, G ^a   Yuying, Z ^a   Daifeng, Z ^a   Lanjie, C ^a   Yu, K ^a  

^a HAINAN MEDICAL UNIVERSITY   (China)

Author keywords

Glucose 6 phosphate dehydrogenase; Glucose 6 phosphate dehydrogenase deficiency; Li nationality; Polymerase chain reaction

Indexed keywords

BIOASSAY; DISEASES; ENZYMES; GENES; MUTAGENESIS;

SINGLE STRAND CONFORMATION POLYMORPHISM ANALYSIS;

GENETIC ENGINEERING;

GLUCOSE 6 PHOSPHATE DEHYDROGENASE; HYDROXYL GROUP; THREONINE;

ARTICLE; CHINESE; COMPARATIVE STUDY; CONTROLLED STUDY; DNA SEQUENCE; ENZYME ACTIVITY; GENE MUTATION; GENETIC SCREENING; GENETIC VARIABILITY; GLUCOSE 6 PHOSPHATE DEHYDROGENASE DEFICIENCY; HUMAN; MAJOR CLINICAL STUDY; MOLECULAR BIOLOGY; SINGLE STRAND CONFORMATION POLYMORPHISM;

CHILD; CHILD, PRESCHOOL; CHINA; FEMALE; GLUCOSEPHOSPHATE DEHYDROGENASE DEFICIENCY; HUMANS; INFANT; MALE; MUTATION;

EID: 0035059462     PISSN: 10039406     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (17)

1. 1376G→T mutation of G6PD gene in the Han and Li nationalities in Hainan, China
2. Molecular characterization of glucose-6-phosphate dehydrogease (G6PD) deficiency by natural and amplification created restriction sites: Five mutations account for most G6PD deficiency cases in Taiwan
3. Molecular characterization of glucose-6-phosphate dehydrogenase deficiency in Chinese infants with or without severe neonatal hyperbilirubinaemia
4. A novel C to T substitution at nucleotide 1360 of cDNA which abolishes a natural Hha I site acounts for a new G6PD deficiency gene in Chinese
5. Molecular characterization of glucose-6-phosphate dehydrogenase (G6PD) deficiency in patients of Chinese decent and identification of new base substitutions in the human G6PD gene
6. G6PD NanKang (517T→C; 173 Phe→Leu): A new Chinese G6PD variant associated with neonatal jaundice
7. Glucose-6-phosphate dehydrogenase mutations causing enzyme deficiency in a model of the tertiary structure of the human enzyme
8. Six point mutations found in Chinese with glucose-6-phosphate dehydrogenase deficiency
9. Gene mutations of glucose-6-phosphate dehydrogenase found in Qianxi, Guizhou
10. G6PD gene mutations in Guangxi, China
11. Molecular characterization glucose-6-phosphate dehydrogenase variants in four ethnic groups in Yunnan province of China
12. Calculating the genetic distance of populations in China by frequencies of 38 gene loci
13. Genetic relationship of populations in China
14. Frequency of glucose-6-phosphate dehydrogenase (G6PD) mutations in Chinese, Filipinos, and Laotians from Hawaii
15. Study on G487A mutation of the glucose-6-phosphate dehydrogenase gene
16. G6PD Mahidol a common deficiency variant in South east Asia is caused by a (163) Glycine-Serine mutation
17. The three-dimensional structure of glucose-6-phosphate dehydrogenase from leuconostoc mesenteroides refined at 2.0 Å resolution