Novel compound heterozygous mutations in ZAP70 in a Chinese patient with leaky severe combined immunodeficiency disorder.

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Novel compound heterozygous mutations in ZAP70 in a Chinese patient with leaky severe combined immunodeficiency disorder.

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2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年論文

@yue

2017年論文

@zh-hant

2017年論文

@zh-hk

2017年論文

@zh-mo

2017年論文

@zh-tw

2017年论文

@wuu

2017年论文

@zh

2017年论文

@zh-cn

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Novel compound heterozygous mu ...... ned immunodeficiency disorder.

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Item

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Novel compound heterozygous mu ...... ned immunodeficiency disorder.

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Novel compound heterozygous mu ...... ned immunodeficiency disorder.

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P1476

Novel compound heterozygous mu ...... ned immunodeficiency disorder.

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P2093

Li-Na Zhou

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Qiao Liu

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Qin Zhao

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Qing Liu

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Xiao-Dong Zhao

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Xiu-Hong Xue

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Xue-Mei Chen

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Xue-Mei Tang

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Yan-Ping Wang

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Yuan Ding

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P2860

ZAP-70: a 70 kd protein-tyrosine kinase that associates with the TCR zeta chain

ZAP70: a master regulator of adaptive immunity

Perinatal lethality and blocked B-cell development in mice lacking the tyrosine kinase Syk

Relation of gene expression phenotype to immunoglobulin mutation genotype in B cell chronic lymphocytic leukemia

Human severe combined immunodeficiency due to a defect in ZAP-70, a T cell tyrosine kinase

ZAP-70 deficiency in an autosomal recessive form of severe combined immunodeficiency

Specific immunoglobulin E responses in ZAP-70-deficient patients are mediated by Syk-dependent T-cell receptor signalling

Syk tyrosine kinase required for mouse viability and B-cell development

Distinct T cell developmental consequences in humans and mice expressing identical mutations in the DLAARN motif of ZAP-70.

Familial CD8 deficiency due to a mutation in the CD8 alpha gene.

P2888

s00251-017-0971-0

P304

199-209

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scholarly article

P356

10.1007/S00251-017-0971-0

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English

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P478

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P577

2017-01-26T00:00:00Z

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P698

28124082

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