MYO9B polymorphisms in multiple sclerosis

Single-nucleotide polymorphisms (SNPs) in the 3′ region of myosin IXB ( MYO9B ) gene have recently been reported to associate with different inflammatory or autoimmune diseases. We monitored for the association of MYO9B variants to multiple sclerosis (MS) in four Northern European populations. First...

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Veröffentlicht in:	European journal of human genetics : EJHG 2009-06, Vol.17 (6), p.840-843
Hauptverfasser:	Kemppinen, Anu, Suvela, Minna, Tienari, Pentti J, Elovaara, Irina, Koivisto, Keijo, Pirttilä, Tuula, Reunanen, Mauri, Rautakorpi, Ilkka, Hillert, Jan, Lundmark, Frida, Oturai, Annette, Ryder, Lars, Harbo, Hanne F, Celius, Elisabeth G, Palotie, Aarno, Daly, Mark, Peltonen, Leena, Saarela, Janna
Format:	Artikel
Sprache:	eng
Schlagworte:	Autoimmune diseases Bioinformatics Biomedical and Life Sciences Biomedicine Case-Control Studies Celiac disease Cytogenetics Diabetes Disease European Continental Ancestry Group - genetics Family Gene Expression Genes Genetics Genotype Haplotypes Health care Hospitals Human Genetics Humans Medicine Multiple sclerosis Multiple Sclerosis - genetics Myosin Myosins - genetics Neurology Neurosciences Polymorphism Polymorphism, Genetic - genetics Population Public health Sclerosis Short Report Single-nucleotide polymorphism
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