No evidence for association of multiple sclerosis with the complement factors C6 and C7.

Chataway, J; Sawcer, S; Sherman, D; Hobart, M; Fernie, B; Coraddu, F; Feakes, R; Broadley, S; Gray, J; Jones, H B; Clayton, D; Goodfellow, P N; Compston, A

Chataway, J; Sawcer, S; Sherman, D; Hobart, M; Fernie, B; Coraddu, F; Feakes, R; Broadley, S; Gray, J; Jones, H B; Clayton, D; Goodfellow, P N; Compston, A.

Affiliation

Chataway J; University of Cambridge Neurology Unit, Addenbrooke's Hospital, UK.

J Neuroimmunol ; 99(1): 150-6, 1999 Sep 01.

Article in En | MEDLINE | ID: mdl-10496188

Subject(s)

Autoimmune Diseases/genetics; Complement C6/genetics; Complement C7/genetics; Multiple Sclerosis/genetics; Case-Control Studies; Female; Gene Frequency; Genetic Linkage; Genetic Predisposition to Disease; Genotype; Haplotypes/genetics; Humans; Linkage Disequilibrium; Male; Point Mutation; Polymorphism, Genetic

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Database: MEDLINE Main subject: Autoimmune Diseases / Complement C6 / Complement C7 / Multiple Sclerosis Type of study: Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Female / Humans / Male Language: En Journal: J Neuroimmunol Year: 1999 Type: Article Affiliation country: United kingdom

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