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

Medicine

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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

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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",

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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.

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Complement-human histocompatibility antigen haplotypes in C2 deficiency

Abstract

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