A novel alpha-thalassemia nonsense mutation in codon 23 of the alpha2-globin gene (GAG-->TAG) in a Tunisian family.
about
Hemoglobinopathies in North Africa: a review.First description in Tunisia of a point mutation at codon 119 (CCT-->TCT) in the alpha1-globin gene: Hb Groene Hart in association with the -alpha3.7 deletion.Mutations on the α2-Globin Gene That May Trigger α(+)-Thalassemia.Alpha+-thalassemia trait caused by a nonsense mutation in the alpha2-globin gene: codon 54 (CAG>TAG).
P2860
A novel alpha-thalassemia nonsense mutation in codon 23 of the alpha2-globin gene (GAG-->TAG) in a Tunisian family.
description
2004 nî lūn-bûn
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2004年の論文
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2004年論文
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2004年論文
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2004年論文
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2004年論文
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2004年論文
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2004年论文
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2004年论文
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2004年论文
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name
A novel alpha-thalassemia nons ...... G-->TAG) in a Tunisian family.
@en
A novel alpha-thalassemia nonsense mutation in codon 23 of the alpha2-globin gene
@nl
type
label
A novel alpha-thalassemia nons ...... G-->TAG) in a Tunisian family.
@en
A novel alpha-thalassemia nonsense mutation in codon 23 of the alpha2-globin gene
@nl
prefLabel
A novel alpha-thalassemia nons ...... G-->TAG) in a Tunisian family.
@en
A novel alpha-thalassemia nonsense mutation in codon 23 of the alpha2-globin gene
@nl
P2093
P2860
P356
P1433
P1476
A novel alpha-thalassemia nons ...... G-->TAG) in a Tunisian family.
@en
P2093
Fadiq Ouali
Hajer Siala
Nathalie Gerard
Rajagopal Krishnamoorthy
Slaheddine Fattoum
Taieb Messaoud
P2860
P304
P356
10.1081/HEM-120040258
P577
2004-08-01T00:00:00Z