Genetic basis of the primary immunodeficiency syndromes.
作者信息
Adelman D C
出版信息
West J Med. 1995 Oct;163(4):373-4.
Abstract
摘要
相似文献
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Genetic basis of the primary immunodeficiency syndromes.原发性免疫缺陷综合征的遗传基础。
West J Med. 1995 Oct;163(4):373-4.
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本文引用的文献
1
The gene involved in X-linked agammaglobulinaemia is a member of the src family of protein-tyrosine kinases.与X连锁无丙种球蛋白血症相关的基因是蛋白质酪氨酸激酶src家族的成员。
Nature. 1993 Jan 21;361(6409):226-33. doi: 10.1038/361226a0.
2
ZAP-70 deficiency in an autosomal recessive form of severe combined immunodeficiency.ZAP-70缺乏症以常染色体隐性形式表现为严重联合免疫缺陷。
Science. 1994 Jun 10;264(5165):1599-601. doi: 10.1126/science.8202713.
3
Human severe combined immunodeficiency due to a defect in ZAP-70, a T cell tyrosine kinase.由于T细胞酪氨酸激酶ZAP-70缺陷导致的人类重症联合免疫缺陷。
Science. 1994 Jun 10;264(5165):1596-9. doi: 10.1126/science.8202712.
4
CD40 ligand gene defects responsible for X-linked hyper-IgM syndrome.导致X连锁高IgM综合征的CD40配体基因缺陷。
Science. 1993 Feb 12;259(5097):990-3. doi: 10.1126/science.7679801.
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