G6PD mahidol, a common deficient variant in South East Asia is caused by a (163)glycine----serine mutation.
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Molecular Analysis of Glucose-6-Phosphate Dehydrogenase Gene Mutations in Bangladeshi Individuals.Identification of a single base change in a new human mutant glucose-6-phosphate dehydrogenase gene by polymerase-chain-reaction amplification of the entire coding region from genomic DNA.Characterization of G6PD genotypes and phenotypes on the northwestern Thailand-Myanmar border.Polymorphic sites in the African population detected by sequence analysis of the glucose-6-phosphate dehydrogenase gene outline the evolution of the variants A and A-.Molecular basis of erythroenzymopathies associated with hereditary hemolytic anemia: tabulation of mutant enzymes.Significance of 3'UTR and Pathogenic Haplotype in Glucose-6-Phosphate Deficiency.
P2860
G6PD mahidol, a common deficient variant in South East Asia is caused by a (163)glycine----serine mutation.
description
1989 nî lūn-bûn
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1989年の論文
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1989年論文
@yue
1989年論文
@zh-hant
1989年論文
@zh-hk
1989年論文
@zh-mo
1989年論文
@zh-tw
1989年论文
@wuu
1989年论文
@zh
1989年论文
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name
G6PD mahidol, a common deficie ...... 63)glycine----serine mutation.
@en
type
label
G6PD mahidol, a common deficie ...... 63)glycine----serine mutation.
@en
prefLabel
G6PD mahidol, a common deficie ...... 63)glycine----serine mutation.
@en
P2093
P356
P1476
G6PD mahidol, a common deficie ...... 63)glycine----serine mutation.
@en
P2093
Luzzatto L
Vulliamy TJ
Wanachiwanawin W
P2860
P356
10.1093/NAR/17.14.5868
P577
1989-07-01T00:00:00Z