Association of the truncating splice site mutation in BTNL2 with multiple sclerosis is secondary to HLA-DRB1*15
Year: 2005
Type: article
Study design: Observational Study
Source: Human Molecular Genetics
DOI: 10.1093/hmg/ddi436
Institution: Wellcome Trust
Language: English
Subfield: Pathology and Forensic Medicine
Field: Medicine
Domain: Health Sciences
Open Access status: closed
OpenAlex ID: W2164859497
