Two French Caucasian families with dominant thalassemia-like phenotypes due to hyper unstable hemoglobin variants: Hb Sainte Seve [codon 118 (-T)] and codon 127 [CAG-->TAG (Gln-->stop]).
about
The molecular basis of β-thalassemia.Production of beta-globin and adult hemoglobin following G418 treatment of erythroid precursor cells from homozygous beta(0)39 thalassemia patients.Dominantly Inherited beta-Thalassemia.Chronic hemolytic anemia due to novel alpha-globin chain variants: critical location of the mutation within the gene sequence for a dominant effect.Development of K562 cell clones expressing beta-globin mRNA carrying the beta039 thalassaemia mutation for the screening of correctors of stop-codon mutations.Hb Stara Zagora: a new hyper-unstable hemoglobin causing severe hemolytic anemia.
P2860
Two French Caucasian families with dominant thalassemia-like phenotypes due to hyper unstable hemoglobin variants: Hb Sainte Seve [codon 118 (-T)] and codon 127 [CAG-->TAG (Gln-->stop]).
description
2005 nî lūn-bûn
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2005年の論文
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2005年学术文章
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2005年学术文章
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2005年学术文章
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2005年学术文章
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2005年学术文章
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2005年学术文章
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2005年學術文章
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2005年學術文章
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name
Two French Caucasian families ...... 127 [CAG-->TAG (Gln-->stop]).
@en
Two French Caucasian families ...... nts: Hb Sainte Seve [codon 118
@nl
type
label
Two French Caucasian families ...... 127 [CAG-->TAG (Gln-->stop]).
@en
Two French Caucasian families ...... nts: Hb Sainte Seve [codon 118
@nl
prefLabel
Two French Caucasian families ...... 127 [CAG-->TAG (Gln-->stop]).
@en
Two French Caucasian families ...... nts: Hb Sainte Seve [codon 118
@nl
P2093
P2860
P356
P1433
P1476
Two French Caucasian families ...... 127 [CAG-->TAG (Gln-->stop]).
@en
P2093
Catherine Le Niger
Claude Préhu
Dora Bachir
Fréderic Galactéros
Henri Wajcman
Maha Al-Sheikh
Serge Pissard
P2860
P304
P356
10.1081/HEM-200066335
P577
2005-01-01T00:00:00Z