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http://purl.uniprot.org/citations/10336779http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/10336779http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/10336779http://www.w3.org/2000/01/rdf-schema#comment"Neurofibromatosis type 1 (NF1) is a dominant disorder caused by mutations in the NF1 gene; approximately 100 NF1 gene mutations have been published. The CpG C-to-T transition is a frequent mutation mechanism in genetic disorders. To estimate its frequency in NF1, we employed a PCR-restriction digestion method to examine 17 CpGs in 65 patients, and also screened for a CpG nonsense transition (R1947X) that occurs in 1-2% of patients. The analysis revealed disease-related CpG C-to-T transitions (including a nonsense mutation that may be as frequent as R1947X) as well as a benign variant and another mutation at a CpG. Four patients showed CpG mutations in analysis of 18 sites (17 surveyed by restriction digest, plus the R1947X assay), including three C-to-T transitions and one C-to-G transversion. These 18 sites represent one-fifth of the 91 CpGs at which a C-to-T transition would result in a nonsense or nonconservative missense mutation. Thus, it is feasible that the CpG mutation rate at NF1 might be similar to that seen in other disorders with a high mutation rate, and that recurrent NF1 mutations may frequently reside at CpG sites."xsd:string
http://purl.uniprot.org/citations/10336779http://purl.org/dc/terms/identifier"doi:10.1002/(sici)1098-1004(1998)11:5<411::aid-humu11>3.0.co;2-2"xsd:string
http://purl.uniprot.org/citations/10336779http://purl.org/dc/terms/identifier"doi:10.1002/(sici)1098-1004(1998)11:5<411::aid-humu11>3.0.co;2-2"xsd:string
http://purl.uniprot.org/citations/10336779http://purl.uniprot.org/core/author"Collins F.S."xsd:string
http://purl.uniprot.org/citations/10336779http://purl.uniprot.org/core/author"Collins F.S."xsd:string
http://purl.uniprot.org/citations/10336779http://purl.uniprot.org/core/author"Driscoll D.J."xsd:string
http://purl.uniprot.org/citations/10336779http://purl.uniprot.org/core/author"Driscoll D.J."xsd:string
http://purl.uniprot.org/citations/10336779http://purl.uniprot.org/core/author"Johnson J.S."xsd:string
http://purl.uniprot.org/citations/10336779http://purl.uniprot.org/core/author"Johnson J.S."xsd:string
http://purl.uniprot.org/citations/10336779http://purl.uniprot.org/core/author"Stalker H.J."xsd:string
http://purl.uniprot.org/citations/10336779http://purl.uniprot.org/core/author"Stalker H.J."xsd:string
http://purl.uniprot.org/citations/10336779http://purl.uniprot.org/core/author"Wallace M.R."xsd:string
http://purl.uniprot.org/citations/10336779http://purl.uniprot.org/core/author"Wallace M.R."xsd:string
http://purl.uniprot.org/citations/10336779http://purl.uniprot.org/core/author"Zori R."xsd:string
http://purl.uniprot.org/citations/10336779http://purl.uniprot.org/core/author"Zori R."xsd:string
http://purl.uniprot.org/citations/10336779http://purl.uniprot.org/core/author"Baumbach L."xsd:string
http://purl.uniprot.org/citations/10336779http://purl.uniprot.org/core/author"Baumbach L."xsd:string
http://purl.uniprot.org/citations/10336779http://purl.uniprot.org/core/author"Williams C.A."xsd:string
http://purl.uniprot.org/citations/10336779http://purl.uniprot.org/core/author"Williams C.A."xsd:string
http://purl.uniprot.org/citations/10336779http://purl.uniprot.org/core/author"Abernathy C.R."xsd:string
http://purl.uniprot.org/citations/10336779http://purl.uniprot.org/core/author"Abernathy C.R."xsd:string
http://purl.uniprot.org/citations/10336779http://purl.uniprot.org/core/author"Kousseff B.G."xsd:string
http://purl.uniprot.org/citations/10336779http://purl.uniprot.org/core/author"Kousseff B.G."xsd:string