Identification of rare genetic variation of NLRP1 gene in familial multiple sclerosis - Maver, Ales; Lavtar, Polona; Ristić, Smiljana; Stopinšek, Sanja; Simčič, Saša; Hočevar, Keli; Sepčić, Juraj; Drulović, Jelena; Pekmezović, Tatjana; Novaković, Ivana; Alenka, Hodžić; Rudolf, Gorazd; et al. (Scientific reports, 2017)
Keywords: 13; 13/21; 45/23; 45/77; 45/91; 631/208/212/2301; 692/4017; Adaptor Proteins, Signal Transducing - genetics; Apoptosis Regulatory Proteins - genetics; Etiology; Evolution, Molecular; Exome; Gene expression; Gene Expression Profiling; Genetic Association Studies; Genetic diversity; Genetic Predisposition to Disease; Genetic Variation; Humanities and Social Sciences; Humans; Interleukin 1; Leukocytes (mononuclear); Melanoma; multidisciplinary; Multiple sclerosis; Multiple Sclerosis - diagnosis; Multiple Sclerosis - genetics; Pedigree; Peripheral blood mononuclear cells; Phylogeny; Science; Science (multidisciplinary); Transcription; Whole Exome Sequencing