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Newly Found C1 Inhibitor Gene Mutation in Hereditary Angioedema Patients
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作者 rui tang hong-yu zhang 《Chinese Medical Sciences Journal》 CAS CSCD 2009年第4期252-252,共1页
Hereditary angioedema (HAE) is an autosomal dominant condition that affects one in about 50 000 persons, characterized by recurrent episodes of subcutaneous or submucosal swelling involving the hands, feet, limbs, f... Hereditary angioedema (HAE) is an autosomal dominant condition that affects one in about 50 000 persons, characterized by recurrent episodes of subcutaneous or submucosal swelling involving the hands, feet, limbs, face, intestinal tract, even larynx and trachea. 展开更多
关键词 hereditary angioedema missense mutation C1 esterase inhibitor
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