CTLA-4 +49 A/G gene polymorphism in Croatian and Slovenian multiple sclerosis patients

Author:

Čizmarević N. Starčević,Gašparović I.,Peterlin B.,Sepčić J.,Rudolf G.,Kapović M.,Lavtar P.,Ristić S.

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine,Immunology

Reference49 articles.

1. [Polymorphism A/G in position +49 of CTLA4 exon 1 in multiple sclerosis in Russians];Andreevskii;Molekuliarnaia Biologiia,2002

2. No evidence for association of CTLA-4 gene polymorphisms with the risk of developing multiple sclerosis: a meta-analysis;Bagos;Multiple Sclerosis,2007

3. Revealing the genetic basis of multiple sclerosis: are we there yet?;Baranzini;Current Opinion in Genetics and Development,2011

4. Progression of multiple sclerosis is associated with exon 1 CTLA-4 gene polymorphism;Bilinska;Acta Neurologica Scandinavica,2004

5. Lack of association between an exon 1 CTLA-4 gene polymorphism A(49)G and multiple sclerosis in a Polish population of the Lower Silesia region;Bocko;Archivum Immunologiae et Therapiae Experimentalis (Warsz),2003

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