Linkage and association with the NOS2A locus on chromosome 17q11 in multiple sclerosis

A large body of research supports a multifactorial cause in multiple sclerosis (MS), with an underlying genetic susceptibility likely acting in concert with undefined environmental exposures. Here, we used a highly efficient multilocus genotyping assay to study single nucleotide polymorphisms repres...

Ausführliche Beschreibung

Gespeichert in:

Bibliographische Detailangaben
Veröffentlicht in:	Annals of neurology 2004-06, Vol.55 (6), p.793-800
Hauptverfasser:	Barcellos, Lisa F., Begovich, Ann B., Reynolds, Rebecca L., Caillier, Stacy J., Brassat, David, Schmidt, Silke, Grams, Sarah E., Walker, Karen, Steiner, Lori L., Cree, Bruce A. C., Stillman, Althea, Lincoln, Robin R., Pericak-Vance, Margaret A., Haines, Jonathan L., Erlich, Henry A., Hauser, Stephen L., Oksenberg, Jorge R.
Format:	Artikel
Sprache:	eng
Schlagworte:	Adult African Americans Biological and medical sciences Case-Control Studies Chromosomes, Human, Pair 17 Exons - genetics Family Health Female Gene Frequency Genetic Predisposition to Disease Genetic Variation Haplotypes HLA-DR2 Antigen Humans Linkage Disequilibrium Male Medical sciences Multiple Sclerosis - epidemiology Multiple Sclerosis - genetics Neurology Nitric Oxide Synthase - genetics Polymorphism, Single Nucleotide
Online-Zugang:	Volltext
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!

Schreiben Sie den ersten Kommentar!