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http://purl.uniprot.org/citations/18041775http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/18041775http://www.w3.org/2000/01/rdf-schema#comment"We report on a novel LMNA mutation (p.R471G) in a proband affected by a syndrome comprising partial lipodystrophy, insulin-resistant diabetes, acanthosis nigricans, liver steatosis, muscle weakness, and contractures. This phenotype has features of both types 1 and 2 familial partial lipodystrophy. The sister and father of the proband had the same mutation. The sister was more mildly affected and the father was apparently unaffected, demonstrating variable expressivity and reduced penetrance for this mutation."xsd:string
http://purl.uniprot.org/citations/18041775http://purl.org/dc/terms/identifier"doi:10.1002/ajmg.a.32046"xsd:string
http://purl.uniprot.org/citations/18041775http://purl.uniprot.org/core/author"Wieacker P."xsd:string
http://purl.uniprot.org/citations/18041775http://purl.uniprot.org/core/author"Jakubiczka S."xsd:string
http://purl.uniprot.org/citations/18041775http://purl.uniprot.org/core/author"Wieland I."xsd:string
http://purl.uniprot.org/citations/18041775http://purl.uniprot.org/core/author"Muschke P."xsd:string
http://purl.uniprot.org/citations/18041775http://purl.uniprot.org/core/author"Brune T."xsd:string
http://purl.uniprot.org/citations/18041775http://purl.uniprot.org/core/author"Kolsch U."xsd:string
http://purl.uniprot.org/citations/18041775http://purl.uniprot.org/core/date"2007"xsd:gYear
http://purl.uniprot.org/citations/18041775http://purl.uniprot.org/core/name"Am J Med Genet A"xsd:string
http://purl.uniprot.org/citations/18041775http://purl.uniprot.org/core/pages"2810-2814"xsd:string
http://purl.uniprot.org/citations/18041775http://purl.uniprot.org/core/title"The heterozygous LMNA mutation p.R471G causes a variable phenotype with features of two types of familial partial lipodystrophy."xsd:string
http://purl.uniprot.org/citations/18041775http://purl.uniprot.org/core/volume"143A"xsd:string
http://purl.uniprot.org/citations/18041775http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/18041775
http://purl.uniprot.org/citations/18041775http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/18041775
http://purl.uniprot.org/uniprot/#_A0A384MQX1-mappedCitation-18041775http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/18041775
http://purl.uniprot.org/uniprot/#_B4DFR3-mappedCitation-18041775http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/18041775
http://purl.uniprot.org/uniprot/#_Q3BDU5-mappedCitation-18041775http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/18041775
http://purl.uniprot.org/uniprot/#_Q8N519-mappedCitation-18041775http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/18041775
http://purl.uniprot.org/uniprot/#_P02545-mappedCitation-18041775http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/18041775
http://purl.uniprot.org/uniprot/#_Q5I6Y5-mappedCitation-18041775http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/18041775
http://purl.uniprot.org/uniprot/#_Q5TCI8-mappedCitation-18041775http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/18041775
http://purl.uniprot.org/uniprot/#_W5X314-mappedCitation-18041775http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/18041775
http://purl.uniprot.org/uniprot/#_W8QEH3-mappedCitation-18041775http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/18041775