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PMID: 7236890 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Kx: its relationship to chronic granulomatous disease and genetic linkage with Xg.

Blood ·Vol. 58 ·No. 1 ·1981-07-00 ·Pages 34-7

Densen P, Wilkinson-Kroovand S, Mandell GL, Sullivan G, Oyen R, Marsh WL

Abstract

The relationship between neutrophil function and the neutrophil antigen, Kx, as well as the linkage of the gene, Xk, with Xg was examined in a kindred with X-linked chronic granulomatous disease. Four of the eight male siblings had chronic granulomatous disease by clinical history and tests of neutrophil function, and all four had Kx-negative neutrophils. The remaining four were in good health and had normal nitroblue tetrazolium reduction tests. However, one of these latter four had Kx-negative neutrophils that functioned normally. These data suggest that closely linked but distinct genes on the X chromosome code for chronic granulomatous disease and Kx. In addition, close linkage was demonstrated between Xk and Xg, a gene coding for an erythrocyte surface antigen.

MeSH Terms
Adult Antigens Blood Grouping and Crossmatching Genetic Linkage Granulomatous Disease, Chronic/genetics Humans Male Middle Aged Neutrophils/immunology Pedigree
Chemicals
Antigens
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Densen P
Wilkinson-Kroovand S
Mandell G L
Sullivan G
Oyen R
Marsh W L
Article Info
Journal
Blood
Abbr.
Blood
ISSN
0006-4971
Published
1981-07-00
Pages
34-7
Language
English
Region
United States
NLM ID
7603509
Subset
IM
Grants
NIAID NIH HHS · AI09504 · United States
NIAID NIH HHS · AI16476 · United States
NHLBI NIH HHS · HL09011 · United States
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