Genetic and functional analyses describe a novel 730delG mutation in the KEL gene causing K0 phenotype in a Taiwanese blood donor.
about
Brain, blood, and iron: perspectives on the roles of erythrocytes and iron in neurodegeneration.Molecular Basis of KELnull Phenotype in Brazilians.Two novel KEL alleles encoding K0 phenotypes in Brazilians.Identification of a novel Kmod -1 allele encoded by 977C>T (Pro326Leu).Identification of novel silent KEL alleles causing KEL:-5 (Ko) phenotype or discordance between KEL:1,-2 phenotype/KEL*01/02 genotype.
P2860
Genetic and functional analyses describe a novel 730delG mutation in the KEL gene causing K0 phenotype in a Taiwanese blood donor.
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年学术文章
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2011年学术文章
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2011年学术文章
@zh-cn
2011年学术文章
@zh-hans
2011年学术文章
@zh-my
2011年学术文章
@zh-sg
2011年學術文章
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2011年學術文章
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name
Genetic and functional analyse ...... pe in a Taiwanese blood donor.
@en
Genetic and functional analyse ...... pe in a Taiwanese blood donor.
@nl
type
label
Genetic and functional analyse ...... pe in a Taiwanese blood donor.
@en
Genetic and functional analyse ...... pe in a Taiwanese blood donor.
@nl
prefLabel
Genetic and functional analyse ...... pe in a Taiwanese blood donor.
@en
Genetic and functional analyse ...... pe in a Taiwanese blood donor.
@nl
P2093
P2860
P1433
P1476
Genetic and functional analyse ...... pe in a Taiwanese blood donor.
@en
P2093
S J L Tsai
P2860
P304
P356
10.1111/J.1365-3148.2011.01084.X
P577
2011-06-26T00:00:00Z