INHERITED COMPLEMENT DEFICIENCIES

被引：32

作者：

LACHMANN, PJ

机构：

来源：

PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY OF LONDON SERIES B-BIOLOGICAL SCIENCES | 1984年 / 306卷 / 1129期

关键词：

D O I：

10.1098/rstb.1984.0102

中图分类号：

Q [生物科学];

学科分类号：

07 ; 0710 ; 09 ;

摘要：

引用

页码：419 / 430

页数：12

共 32 条

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PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1983, 80 (06) :1698-1702

[4] PREVALENCE OF CONGENITAL OR ACQUIRED COMPLEMENT DEFICIENCY IN PATIENTS WITH SPORADIC MENINGOCOCCAL DISEASE [J].

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KOHLER, PF ;

CURD, JG ;

JUDSON, FN ;

RELLER, LB .

NEW ENGLAND JOURNAL OF MEDICINE, 1983, 308 (16) :913-916

[5] FAMILY STUDY OF THE MAJOR HISTOCOMPATIBILITY COMPLEX IN PATIENTS WITH SYSTEMIC LUPUS-ERYTHEMATOSUS - IMPORTANCE OF NULL ALLELES OF C4A AND C4B IN DETERMINING DISEASE SUSCEPTIBILITY [J].

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[6]

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[7]

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[9]

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[10]

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