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http://purl.uniprot.org/citations/18762705http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/18762705http://www.w3.org/2000/01/rdf-schema#comment"Brugada syndrome is an inherited arrhythmic disorder, and mutations in the SCN5A gene, encoding cardiac sodium channels, are identified in approximately 15% of cases. A novel causative gene (glycerol-3 phosphate dehydrogenase-1 like; GPD1L) has been reported, and in the present study, 80 unrelated Japanese patients were screened for GPD1L mutations: 1 synonymous mutation was identified, as well as 1 intronic variant, both of which were absent in 220 control alleles. Additionally, a single-nucleotide polymorphism was detected in 4 patients. No non-synonymous mutations were found. GPD1L does not appear to be a major cause of Brugada syndrome in the Japanese population."xsd:string
http://purl.uniprot.org/citations/18762705http://purl.org/dc/terms/identifier"doi:10.1253/circj.cj-08-0508"xsd:string
http://purl.uniprot.org/citations/18762705http://purl.uniprot.org/core/author"Horie M."xsd:string
http://purl.uniprot.org/citations/18762705http://purl.uniprot.org/core/author"Nishio Y."xsd:string
http://purl.uniprot.org/citations/18762705http://purl.uniprot.org/core/author"Ohno S."xsd:string
http://purl.uniprot.org/citations/18762705http://purl.uniprot.org/core/author"Tsuji K."xsd:string
http://purl.uniprot.org/citations/18762705http://purl.uniprot.org/core/author"Kita T."xsd:string
http://purl.uniprot.org/citations/18762705http://purl.uniprot.org/core/author"Doi T."xsd:string
http://purl.uniprot.org/citations/18762705http://purl.uniprot.org/core/author"Akao M."xsd:string
http://purl.uniprot.org/citations/18762705http://purl.uniprot.org/core/author"Makiyama T."xsd:string
http://purl.uniprot.org/citations/18762705http://purl.uniprot.org/core/author"Haruna Y."xsd:string
http://purl.uniprot.org/citations/18762705http://purl.uniprot.org/core/date"2008"xsd:gYear
http://purl.uniprot.org/citations/18762705http://purl.uniprot.org/core/name"Circ J"xsd:string
http://purl.uniprot.org/citations/18762705http://purl.uniprot.org/core/pages"1705-1706"xsd:string
http://purl.uniprot.org/citations/18762705http://purl.uniprot.org/core/title"Mutation analysis of the glycerol-3 phosphate dehydrogenase-1 like (GPD1L) gene in Japanese patients with Brugada syndrome."xsd:string
http://purl.uniprot.org/citations/18762705http://purl.uniprot.org/core/volume"72"xsd:string
http://purl.uniprot.org/citations/18762705http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/18762705
http://purl.uniprot.org/citations/18762705http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/18762705
http://purl.uniprot.org/uniprot/#_B3KWN2-mappedCitation-18762705http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/18762705
http://purl.uniprot.org/uniprot/#_Q8N335-mappedCitation-18762705http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/18762705
http://purl.uniprot.org/uniprot/B3KWN2http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/18762705
http://purl.uniprot.org/uniprot/Q8N335http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/18762705