Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Sclerosis and BTNL2[original query] |
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Association of the truncating splice site mutation in BTNL2 with multiple sclerosis is secondary to HLA-DRB1*15. Human molecular genetics 2006 Jan 15 (1): 155-61. Traherne James A, Barcellos Lisa F, Sawcer Stephen J, Compston Alastair, Ramsay Patricia P, Hauser Stephen L, Oksenberg Jorge R, Trowsdale Jo |
HLA-DRA/HLA-DRB5 polymorphism affects risk of sporadic ALS and survival in a southwest Chinese cohort. Journal of the neurological sciences 2017 Feb 373 124-128. Yang Xinglong, Zheng JinHua, Tian Sijia, Chen Yalan, An Ran, Zhao Quanzhen, Xu Yanmi |
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- Page last updated:Apr 16, 2024
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