CYSTIC-FIBROSIS - A SEARCH FOR THE BASIC DEFECT

被引：0

作者：

KOLLBERG, H ^{[1
]}

BARDON, A ^{[1
]}

CEDER, O ^{[1
]}

机构：

[1] UMEA UNIV HOSP,DEPT PEDIAT,S-90185 UMEA,SWEDEN

来源：

CLINICAL GENETICS | 1986年 / 29卷 / 05期

关键词：

D O I：

暂无

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：463 / 464

页数：2

共 50 条

[31] NA+ TRANSPORT DEFECT IN CYSTIC-FIBROSIS
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[32] POSSIBILITY OF A SPECIFIC ANDROGEN DEFECT IN CYSTIC-FIBROSIS
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[33] CYSTIC-FIBROSIS - DIAGNOSTIC TESTING AND THE SEARCH FOR THE GENE
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[34] CYSTIC-FIBROSIS - MANAGEMENT OF THE CHILD WITH CYSTIC-FIBROSIS
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[35] ALTERED REGULATION OF A PROTEINASE MEDIATED PRIMARY SECRETION PROCESSING SYSTEM AS THE BASIC DEFECT IN CYSTIC-FIBROSIS
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[36] Pharmacological treatment of the basic defect in cystic fibrosis
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[37] Therapies directed at the basic defect in cystic fibrosis
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[38] Cystic fibrosis treatment: targeting the basic defect
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[39] ABSENCE OF ELECTROCHEMICAL DEFECT OF CYSTIC-FIBROSIS IN TRANSPLANTED LUNG
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[40] CYSTIC-FIBROSIS DOES NOT INVOLVE A DEFECT IN CAPNOPHORIN FUNCTION
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