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http://purl.uniprot.org/citations/20799326http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/20799326http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/20799326http://www.w3.org/2000/01/rdf-schema#comment"Dursun syndrome is a triad of familial primary pulmonary hypertension, leucopenia, and atrial septal defect. Here we demonstrate that mutations in G6PC3 cause Dursun syndrome. Mutations in G6PC3 are known to also cause severe congenital neutropenia type 4. Identification of the genetic basis of Dursun syndrome expands the pre-existing knowledge about the phenotypic effects of mutations in G6PC3. We propose that Dursun syndrome should now be considered as a subset of severe congenital neutropenia type 4 with pulmonary hypertension as an important clinical feature."xsd:string
http://purl.uniprot.org/citations/20799326http://purl.org/dc/terms/identifier"doi:10.1002/ajmg.a.33615"xsd:string
http://purl.uniprot.org/citations/20799326http://purl.org/dc/terms/identifier"doi:10.1002/ajmg.a.33615"xsd:string
http://purl.uniprot.org/citations/20799326http://purl.uniprot.org/core/author"Newman W.G."xsd:string
http://purl.uniprot.org/citations/20799326http://purl.uniprot.org/core/author"Newman W.G."xsd:string
http://purl.uniprot.org/citations/20799326http://purl.uniprot.org/core/author"Banka S."xsd:string
http://purl.uniprot.org/citations/20799326http://purl.uniprot.org/core/author"Banka S."xsd:string
http://purl.uniprot.org/citations/20799326http://purl.uniprot.org/core/author"Dursun A."xsd:string
http://purl.uniprot.org/citations/20799326http://purl.uniprot.org/core/author"Dursun A."xsd:string
http://purl.uniprot.org/citations/20799326http://purl.uniprot.org/core/author"Ozgul R.K."xsd:string
http://purl.uniprot.org/citations/20799326http://purl.uniprot.org/core/author"Ozgul R.K."xsd:string
http://purl.uniprot.org/citations/20799326http://purl.uniprot.org/core/date"2010"xsd:gYear
http://purl.uniprot.org/citations/20799326http://purl.uniprot.org/core/date"2010"xsd:gYear
http://purl.uniprot.org/citations/20799326http://purl.uniprot.org/core/name"Am. J. Med. Genet. A"xsd:string
http://purl.uniprot.org/citations/20799326http://purl.uniprot.org/core/name"Am. J. Med. Genet. A"xsd:string
http://purl.uniprot.org/citations/20799326http://purl.uniprot.org/core/pages"2609-2611"xsd:string
http://purl.uniprot.org/citations/20799326http://purl.uniprot.org/core/pages"2609-2611"xsd:string
http://purl.uniprot.org/citations/20799326http://purl.uniprot.org/core/title"Mutations in the G6PC3 gene cause Dursun syndrome."xsd:string
http://purl.uniprot.org/citations/20799326http://purl.uniprot.org/core/title"Mutations in the G6PC3 gene cause Dursun syndrome."xsd:string
http://purl.uniprot.org/citations/20799326http://purl.uniprot.org/core/volume"152"xsd:string
http://purl.uniprot.org/citations/20799326http://purl.uniprot.org/core/volume"152"xsd:string
http://purl.uniprot.org/citations/20799326http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/20799326
http://purl.uniprot.org/citations/20799326http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/20799326