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Volumn 73, Issue 7, 2016, Pages 795-802

Association of HLA genetic risk burden with disease phenotypes in multiple sclerosis

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; BRAIN ATROPHY; BRAIN DAMAGE; CASE CONTROL STUDY; CERVICAL SPINAL CORD; CONTROLLED STUDY; CROSS-SECTIONAL STUDY; DISEASE COURSE; DISEASE DURATION; DISEASE SEVERITY; FEMALE; GENETIC ASSOCIATION; GENETIC RISK; GRAY MATTER; HAPLOTYPE; HLA SYSTEM; HUMAN; MAJOR CLINICAL STUDY; MALE; MULTIPLE SCLEROSIS; NEUROPROTECTION; NUCLEAR MAGNETIC RESONANCE IMAGING; ONSET AGE; OUTCOME ASSESSMENT; PHENOTYPE; PRIORITY JOURNAL; SPINAL CORD; WHITE MATTER; ALLELE; BRAIN; CAUCASIAN; DIAGNOSTIC IMAGING; GENETIC ASSOCIATION STUDY; GENETIC PREDISPOSITION; GENETICS; MIDDLE AGED; PATHOLOGY; PATHOPHYSIOLOGY; RETROSPECTIVE STUDY; SINGLE NUCLEOTIDE POLYMORPHISM; THREE DIMENSIONAL IMAGING; YOUNG ADULT;

EID: 84978141630     PISSN: 21686149     EISSN: None     Source Type: Journal    
DOI: 10.1001/jamaneurol.2016.0980     Document Type: Article
Times cited : (65)

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