Abstract
= 0.05). Examination of individual alleles within these haplotypes implicated P2X7R and CAMKK2 in pathways affecting pulmonary NTM disease.
Halstrom S, Cherry CL, Black M, Thomson R, Goullee H, Baltic S, Allcock R, Temple SEL, Price P
VIEW FULL ARTICLEJournal Immunogenetics
Published 23 Feb 2017
Volume 69
ISSUE 5
Pagination 287-293
DOI 10.1007/s00251-017-0972-z
= 0.05). Examination of individual alleles within these haplotypes implicated P2X7R and CAMKK2 in pathways affecting pulmonary NTM disease.