Comprehensive investigation of RNF213 nonsynonymous variants associated with intracranial artery stenosis - Hongo, Hiroki; Miyawaki, Satoru; Imai, Hideaki; Shimizu, Masahiro; Yagi, Shinichi; Mitsui, Jun; Ishiura, Hiroyuki; Yoshimura, Jun; Doi, Koichiro; Qu, Wei; Teranishi, Yu; Okano, Atsushi; et al. (Scientific reports, 2020)
Keywords: 692/4017; 692/499; Adenosine Triphosphatases - genetics; Adolescent; Adult; Aged; Aged, 80 and over; Alleles; Amino Acid Substitution; Biotechnology; Blood pressure; Cardiovascular disease; Constriction, Pathologic - etiology; Constriction, Pathologic - pathology; Diabetes; Exons; Female; Gene polymorphism; Genetic Association Studies; Genetic Predisposition to Disease; Genetic Variation; Genomes; Genotype; Hospitals; Humanities and Social Sciences; Humans; Hypertension; Intracranial Arterial Diseases - diagnostic imaging; Intracranial Arterial Diseases - genetics; Intracranial Arterial Diseases - pathology; Ischemia; Male; Medicine; Middle Aged; Moyamoya disease; multidisciplinary; Mutation, Missense; Neurosurgery; Polymorphism, Single Nucleotide; Population; Proteins; Racial differences; Science; Science (multidisciplinary); Sequence Analysis, DNA; Single-nucleotide polymorphism; Stenosis; Stroke; Ubiquitin-Protein Ligases - genetics; Young Adult