Complement-human histocompatibility antigen haplotypes in C2 deficiency

Z. L. Awdeh; D. D. Raum; D. Glass; V. Agnello; P. H. Schur; R. B. Johnston; E. W. Gelfand; M. Ballow; E. Yunis; C. A. Alper

doi:10.1172/JCI110070

Complement-human histocompatibility antigen haplotypes in C2 deficiency

Z. L. Awdeh
, D. D. Raum
, D. Glass
, V. Agnello
, P. H. Schur
, R. B. Johnston
, E. W. Gelfand
, M. Ballow
, E. Yunis
, C. A. Alper

Pediatrics

Brigham and Women’s Hospital

Research output: Contribution to journal › Article › peer-review

47 Scopus citations

Abstract

C4 allotyping 13 homozygous C2-deficient individuals demonstrated 23 of 25 haplotypes to be of the relatively rare type C4A-4 B-2. This is of the same magnitude as the association of C2-Q0 with HLA-DW2/DR2.

Original language	English
Pages (from-to)	581-583
Number of pages	3
Journal	Unknown Journal
Volume	67
Issue number	2
DOIs	https://doi.org/10.1172/JCI110070
State	Published - 1981

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10.1172/JCI110070

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@article{597497638a224946bddc2ecefd569036,

title = "Complement-human histocompatibility antigen haplotypes in C2 deficiency",

abstract = "C4 allotyping 13 homozygous C2-deficient individuals demonstrated 23 of 25 haplotypes to be of the relatively rare type C4A-4 B-2. This is of the same magnitude as the association of C2-Q0 with HLA-DW2/DR2.",

author = "Awdeh, \{Z. L.\} and Raum, \{D. D.\} and D. Glass and V. Agnello and Schur, \{P. H.\} and Johnston, \{R. B.\} and Gelfand, \{E. W.\} and M. Ballow and E. Yunis and Alper, \{C. A.\}",

year = "1981",

doi = "10.1172/JCI110070",

language = "English",

volume = "67",

pages = "581--583",

journal = "Unknown Journal",

number = "2",

}

TY - JOUR

T1 - Complement-human histocompatibility antigen haplotypes in C2 deficiency

AU - Awdeh, Z. L.

AU - Raum, D. D.

AU - Glass, D.

AU - Agnello, V.

AU - Schur, P. H.

AU - Johnston, R. B.

AU - Gelfand, E. W.

AU - Ballow, M.

AU - Yunis, E.

AU - Alper, C. A.

PY - 1981

Y1 - 1981

N2 - C4 allotyping 13 homozygous C2-deficient individuals demonstrated 23 of 25 haplotypes to be of the relatively rare type C4A-4 B-2. This is of the same magnitude as the association of C2-Q0 with HLA-DW2/DR2.

AB - C4 allotyping 13 homozygous C2-deficient individuals demonstrated 23 of 25 haplotypes to be of the relatively rare type C4A-4 B-2. This is of the same magnitude as the association of C2-Q0 with HLA-DW2/DR2.

UR - https://www.scopus.com/pages/publications/0019474493

U2 - 10.1172/JCI110070

DO - 10.1172/JCI110070

M3 - Article

AN - SCOPUS:0019474493

VL - 67

SP - 581

EP - 583

JO - Unknown Journal

JF - Unknown Journal

IS - 2

ER -

Complement-human histocompatibility antigen haplotypes in C2 deficiency

Abstract

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