ALPHA-1-ANTITRYPSIN DEFICIENCY AND EMPHYSEMA CAUSED BY HOMOZYGOUS INHERITANCE OF NON-EXPRESSING ALPHA-1-ANTITRYPSIN GENES

被引：85

作者：

GARVER, RI ^{[1
]}

MORNEX, JF ^{[1
]}

NUKIWA, T ^{[1
]}

BRANTLY, M ^{[1
]}

COURTNEY, M ^{[1
]}

LECOCQ, JP ^{[1
]}

CRYSTAL, RG ^{[1
]}

机构：

[1] TRANSGENE SA, F-6700 STRASBOURG, FRANCE

来源：

NEW ENGLAND JOURNAL OF MEDICINE | 1986年 / 314卷 / 12期

关键词：

D O I：

10.1056/NEJM198603203141207

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：762 / 766

页数：5

共 59 条

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[9] INTERRELATIONSHIPS BETWEEN HUMAN ALVEOLAR MACROPHAGE AND ALPHA-1-ANTITRYPSIN
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[10] HIGH-LEVEL PRODUCTION OF BIOLOGICALLY-ACTIVE HUMAN ALPHA-1-ANTITRYPSIN IN ESCHERICHIA-COLI
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