Hereditary Red Cell Membrane Disorders in Japan: Their Genotypic and Phenotypic Features in 1014 Cases Studied.

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Hereditary Red Cell Membrane Disorders in Japan: Their Genotypic and Phenotypic Features in 1014 Cases Studied.

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2001 nî lūn-bûn

@nan

2001年の論文

@ja

2001年学术文章

@wuu

2001年学术文章

@zh-cn

2001年学术文章

@zh-hans

2001年学术文章

@zh-my

2001年学术文章

@zh-sg

2001年學術文章

@yue

2001年學術文章

@zh

2001年學術文章

@zh-hant

name

Hereditary Red Cell Membrane D ...... eatures in 1014 Cases Studied.

@en

Hereditary Red Cell Membrane D ...... eatures in 1014 Cases Studied.

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type

Item

label

Hereditary Red Cell Membrane D ...... eatures in 1014 Cases Studied.

@en

Hereditary Red Cell Membrane D ...... eatures in 1014 Cases Studied.

@nl

prefLabel

Hereditary Red Cell Membrane D ...... eatures in 1014 Cases Studied.

@en

Hereditary Red Cell Membrane D ...... eatures in 1014 Cases Studied.

@nl

P1476

Hereditary Red Cell Membrane D ...... eatures in 1014 Cases Studied.

@en

P2093

A Kanzaki

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A Yawata

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H Nakanishi

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M Kaku

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Y Yawata

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P2860

Targeted disruption of the murine erythroid band 3 gene results in spherocytosis and severe haemolytic anaemia despite a normal membrane skeleton

Ankyrin-1 mutations are a major cause of dominant and recessive hereditary spherocytosis

Deletion in erythrocyte band 3 gene in malaria-resistant Southeast Asian ovalocytosis

Homozygous 4.1(-) hereditary elliptocytosis associated with a point mutation in the downstream initiation codon of protein 4.1 gene

Human lecithin-cholesterol acyltransferase gene: complete gene sequence and sites of expression

Molecular analysis of insertion/deletion mutations in protein 4.1 in elliptocytosis. II. Determination of molecular genetic origins of rearrangements

A 5' splice region G-->C mutation in exon 3 of the human beta-spectrin gene leads to decreased levels of beta-spectrin mRNA and is responsible for dominant hereditary spherocytosis (spectrin Guemene-Penfao)

Erythrocyte spectrin is comprised of many homologous triple helical segments

Hereditary stomatocytosis: consistent association with an integral membrane protein deficiency

A point mutation in the protein 4.2 gene (allele 4.2 Tozeur) associated with hereditary haemolytic anaemia

P304

399-422

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P31

scholarly article

P356

10.1080/10245332.2001.11746596

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P433

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P478

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P577

2001-01-01T00:00:00Z

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P698

27405697

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