Exome and regulatory element sequencing of neuromyelitis optica patients

Abstract Neuromyelitis optica (NMO) is rare in Finland. To identify rare genetic variants contributing to NMO risk we performed whole exome, HLA and regulatory region sequencing in all ascertained cases during 2005–2013 (n = 5) in a Southern Finnish population of 1.6 million. There were no rare vari...

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