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

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

42 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 (US)
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
Externally published	Yes

ASJC Scopus subject areas

Medicine(all)

Access to Document

10.1172/JCI110070

Cite this

@article{a695521320be4b86943763e43f8d44a8,

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 (US)",

volume = "67",

pages = "581--583",

journal = "Journal of Trace Elements in Medicine and Biology",

issn = "0946-672X",

publisher = "Urban und Fischer Verlag GmbH und Co. KG",

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 - http://www.scopus.com/inward/record.url?scp=0019474493&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0019474493&partnerID=8YFLogxK

U2 - 10.1172/JCI110070

DO - 10.1172/JCI110070

M3 - Article

C2 - 7462431

AN - SCOPUS:0019474493

SN - 0946-672X

VL - 67

SP - 581

EP - 583

JO - Journal of Trace Elements in Medicine and Biology

JF - Journal of Trace Elements in Medicine and Biology

IS - 2

ER -

Complement-human histocompatibility antigen haplotypes in C2 deficiency

Abstract

ASJC Scopus subject areas

Access to Document

Other files and links

Fingerprint

Cite this