C2 DEFICIENCY AND A LUPUS ERYTHEMATOSUS-LIKE ILLNESS - FAMILY RE-EVALUATION

被引：14

作者：

WAHL, R

MEO, T

SHREFFLER, D

MILLER, W

ATKINSON, JP

SCHULTZ, J

OSTERLAND, CK

机构：

[1] UNIV MICHIGAN, MED CTR, ANN ARBOR, MI 48104 USA

[2] MCGILL UNIV, SCH MED, MONTREAL H3A 1A1, QUEBEC, CANADA

来源：

ANNALS OF INTERNAL MEDICINE | 1979年 / 90卷 / 04期

关键词：

D O I：

10.7326/0003-4819-90-4-717_3

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：717 / 718

页数：2

共 5 条

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[2] COMPLEMENT GENETICS IN RELATION TO HLA [J].

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HOBART, MJ .

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[3] STRUCTURAL HETEROGENEITY OF C2 COMPLEMENT PROTEIN AND ITS GENETIC-VARIANTS IN MAN - NEW POLYMORPHISM OF HLA REGION [J].

MEO, T ;

ATKINSON, JP ;

BERNOCO, M ;

BERNOCO, D ;

CEPPELLINI, R .

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1977, 74 (04) :1672-1675

[4] INHERITED C2 DEFICIENCY AND SYSTEMIC LUPUS-ERYTHEMATOSUS - STUDIES ON A FAMILY [J].

OSTERLAND, CK ;

ESPINOZA, L ;

PARKER, LP ;

SCHUR, PH .

ANNALS OF INTERNAL MEDICINE, 1975, 82 (03) :323-328

[5]

PARISER KM, 1978, J IMMUNOL, V121, P2580

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