Correlation between platelet phenotype and NBEAL2 genotype in patients with congenital thrombocytopenia and α-granule deficiency.

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作者： Roberta,Bottega ^[1] ; Alessandro,Pecci ; Erica,De Candia ; Nuria,Pujol-Moix ; Paula G,Heller ; Patrizia,Noris ; Daniela,De Rocco ; Gian Marco,Podda ; Ana C,Glembotsky ; Marco,Cattaneo ; Carlo L,Balduini ; Anna,Savoia

作者单位： Department of Medical Sciences, University of Trieste, Trieste, Italy. ^[1]

主题词等位基因(Alleles);血小板(Blood Platelets);血蛋白质类(Blood Proteins);外显子(Exons);遗传关联研究(Genetic Association Studies);基因型(Genotype);灰色血小板综合征(Gray Platelet Syndrome);单倍剂量不足(Haploinsufficiency);人类(Humans);内含子(Introns);突变(Mutation);系谱(Pedigree);表型(Phenotype);RNA剪接(RNA Splicing)

DOI 10.3324/haematol.2012.075861

PMID 23100277

发布时间 2021-10-21

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Haematologica

2013年98卷6期

868-74页

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Correlation between platelet phenotype and NBEAL2 genotype in patients with congenital thrombocytopenia and α-granule deficiency.

Haematologica

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Haematologica

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Correlation between platelet phenotype and NBEAL2 genotype in patients with congenital thrombocytopenia and α-granule deficiency.

Haematologica

相似文献

Haematologica

相关期刊

检索历史清除