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http://purl.uniprot.org/citations/24357026http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/24357026http://www.w3.org/2000/01/rdf-schema#comment"The major cause of lipid storage myopathies (LSM) in China is multiple acyl-CoA dehydrogenase deficiency (MADD) caused by ETFDH mutations. We here present an analysis of the spectrum of ETFDH mutations in the largest cohort of patients with MADD (90 unrelated patients). We identified 61 ETFDH mutations, including 31 novel mutations, which were widely distributed within the coding sequence. Three frequent mutations were identified: c.250G > A (most common in South China), c.770A > G and c.1227A > C (most common in both South and North China). Regional differences of allele frequency and further haplotype analysis suggest the possibility of founder effects of c.250G > A and c.770A > G. These findings promise to provide the basis for implementing a rapid and economical strategy for diagnosing MADD."xsd:string
http://purl.uniprot.org/citations/24357026http://purl.org/dc/terms/identifier"doi:10.1007/s10545-013-9671-6"xsd:string
http://purl.uniprot.org/citations/24357026http://purl.uniprot.org/core/author"Lin J."xsd:string
http://purl.uniprot.org/citations/24357026http://purl.uniprot.org/core/author"Lu J."xsd:string
http://purl.uniprot.org/citations/24357026http://purl.uniprot.org/core/author"Luo S."xsd:string
http://purl.uniprot.org/citations/24357026http://purl.uniprot.org/core/author"Li D."xsd:string
http://purl.uniprot.org/citations/24357026http://purl.uniprot.org/core/author"Zhao C."xsd:string
http://purl.uniprot.org/citations/24357026http://purl.uniprot.org/core/author"Zhu W."xsd:string
http://purl.uniprot.org/citations/24357026http://purl.uniprot.org/core/author"Yan C."xsd:string
http://purl.uniprot.org/citations/24357026http://purl.uniprot.org/core/author"Xi J."xsd:string
http://purl.uniprot.org/citations/24357026http://purl.uniprot.org/core/author"Lin P."xsd:string
http://purl.uniprot.org/citations/24357026http://purl.uniprot.org/core/author"Wen B."xsd:string
http://purl.uniprot.org/citations/24357026http://purl.uniprot.org/core/date"2014"xsd:gYear
http://purl.uniprot.org/citations/24357026http://purl.uniprot.org/core/name"J Inherit Metab Dis"xsd:string
http://purl.uniprot.org/citations/24357026http://purl.uniprot.org/core/pages"399-404"xsd:string
http://purl.uniprot.org/citations/24357026http://purl.uniprot.org/core/title"Clinical features and ETFDH mutation spectrum in a cohort of 90 Chinese patients with late-onset multiple acyl-CoA dehydrogenase deficiency."xsd:string
http://purl.uniprot.org/citations/24357026http://purl.uniprot.org/core/volume"37"xsd:string
http://purl.uniprot.org/citations/24357026http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/24357026
http://purl.uniprot.org/citations/24357026http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/24357026
http://purl.uniprot.org/uniprot/#_A0A3G6ZET5-mappedCitation-24357026http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/24357026
http://purl.uniprot.org/uniprot/#_A0A2I6U1K5-mappedCitation-24357026http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/24357026
http://purl.uniprot.org/uniprot/#_A0A2I6U1Q3-mappedCitation-24357026http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/24357026
http://purl.uniprot.org/uniprot/#_A7UNU5-mappedCitation-24357026http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/24357026
http://purl.uniprot.org/uniprot/#_A7UNU6-mappedCitation-24357026http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/24357026