Novel dominant β-thalassemia: Hb Boston-Kuwait [codon 139/140(+T)].

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Genome at juncture of early human migration: a systematic analysis of two whole genomes and thirteen exomes from Kuwaiti population subgroup of inferred Saudi Arabian tribe ancestry.Diverse hematological phenotypes of β-thalassemia carriers.

P2860

Q30437010-CD121D33-C54F-4A14-9957-C8B2F7F6D845 Q38819788-65BF6E3E-375E-4A9A-970B-297A51C1B19E

P2860

Novel dominant β-thalassemia: Hb Boston-Kuwait [codon 139/140(+T)].

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http://www.wikidata.org/entity/Q50898967

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2013 nî lūn-bûn

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2013年の論文

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2013年学术文章

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2013年学术文章

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2013年学术文章

@zh-cn

2013年学术文章

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2013年学术文章

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Novel dominant β-thalassemia: Hb Boston-Kuwait [codon 139/140

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Novel dominant β-thalassemia: Hb Boston-Kuwait [codon 139/140(+T)].

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type

Item

label

Novel dominant β-thalassemia: Hb Boston-Kuwait [codon 139/140

@nl

Novel dominant β-thalassemia: Hb Boston-Kuwait [codon 139/140(+T)].

@en

prefLabel

Novel dominant β-thalassemia: Hb Boston-Kuwait [codon 139/140

@nl

Novel dominant β-thalassemia: Hb Boston-Kuwait [codon 139/140(+T)].

@en

P1476

Novel dominant β-thalassemia: Hb Boston-Kuwait [codon 139/140(+T)]

@en

P2093

Leslie E Lehmann

http://www.w3.org/2001/XMLSchema#string

P2860

Dominantly inherited beta thalassaemia intermedia caused by a new single nucleotide deletion in exon 2 of the beta globin gene: Hb morgantown (beta91 CTG>CG)

Dominant beta thalassaemia: molecular basis and pathophysiology.

Genetic modifiers of β-thalassemia and clinical severity as assessed by age at first transfusion.

Dominantly Inherited beta-Thalassemia.

Hematopoietic cell transplantation for thalassemia and sickle cell disease: past, present and future.

A spontaneous deletion of beta 33/34 Val in exon 2 of the beta globin gene (Hb Korea) produces the phenotype of dominant beta thalassaemia.

Dominant beta-thalassemia due to a newly identified frameshift mutation in exon 3 (codon 113, GTG-->Tg).

Hb Stara Zagora: a new hyper-unstable hemoglobin causing severe hemolytic anemia.

Dominant beta-thalassaemia: a highly unstable haemoglobin is caused by a novel 6 bp deletion of the beta-globin gene.

P304

E131-4

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scholarly article

P356

10.1002/PBC.24611

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P478

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2013-06-15T00:00:00Z

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23776097

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Novel dominant β-thalassemia: Hb Boston-Kuwait [codon 139/140(+T)].

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P2860

P2860

Novel dominant β-thalassemia: Hb Boston-Kuwait [codon 139/140(+T)].

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type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698