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http://purl.uniprot.org/citations/11748854http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/11748854http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/11748854http://www.w3.org/2000/01/rdf-schema#comment"Pendred syndrome is an autosomal-recessive disorder characterized by congenital sensorineural hearing loss combined with goiter. This disorder may account for up to 10% of cases of hereditary deafness. The disease gene (PDS/SLC26A4) has been mapped to chromosome 7q22-q31 and encodes a chloride-iodide transport protein. Mutations in this gene are also a cause of non-syndromic autosomal recessive hearing impairment (DFNB4). We have analyzed the PDS/SLC26A4 gene in Spanish and Italian families and we have detected five new mutations (X871M, T132I, IVS1-2A>G, Y556H and 406del5)."xsd:string
http://purl.uniprot.org/citations/11748854http://purl.org/dc/terms/identifier"doi:10.1002/humu.1238"xsd:string
http://purl.uniprot.org/citations/11748854http://purl.org/dc/terms/identifier"doi:10.1002/humu.1238"xsd:string
http://purl.uniprot.org/citations/11748854http://purl.uniprot.org/core/author"Estivill X."xsd:string
http://purl.uniprot.org/citations/11748854http://purl.uniprot.org/core/author"Estivill X."xsd:string
http://purl.uniprot.org/citations/11748854http://purl.uniprot.org/core/author"Lopez-Bigas N."xsd:string
http://purl.uniprot.org/citations/11748854http://purl.uniprot.org/core/author"Lopez-Bigas N."xsd:string
http://purl.uniprot.org/citations/11748854http://purl.uniprot.org/core/author"Gasparini P."xsd:string
http://purl.uniprot.org/citations/11748854http://purl.uniprot.org/core/author"Gasparini P."xsd:string
http://purl.uniprot.org/citations/11748854http://purl.uniprot.org/core/author"Melchionda S."xsd:string
http://purl.uniprot.org/citations/11748854http://purl.uniprot.org/core/author"Melchionda S."xsd:string
http://purl.uniprot.org/citations/11748854http://purl.uniprot.org/core/author"Zelante L."xsd:string
http://purl.uniprot.org/citations/11748854http://purl.uniprot.org/core/author"Zelante L."xsd:string
http://purl.uniprot.org/citations/11748854http://purl.uniprot.org/core/author"Arbones M.L."xsd:string
http://purl.uniprot.org/citations/11748854http://purl.uniprot.org/core/author"Arbones M.L."xsd:string
http://purl.uniprot.org/citations/11748854http://purl.uniprot.org/core/author"de Cid R."xsd:string
http://purl.uniprot.org/citations/11748854http://purl.uniprot.org/core/author"de Cid R."xsd:string
http://purl.uniprot.org/citations/11748854http://purl.uniprot.org/core/author"Grifa A."xsd:string
http://purl.uniprot.org/citations/11748854http://purl.uniprot.org/core/author"Grifa A."xsd:string
http://purl.uniprot.org/citations/11748854http://purl.uniprot.org/core/author"Govea N."xsd:string
http://purl.uniprot.org/citations/11748854http://purl.uniprot.org/core/author"Govea N."xsd:string
http://purl.uniprot.org/citations/11748854http://purl.uniprot.org/core/date"2001"xsd:gYear
http://purl.uniprot.org/citations/11748854http://purl.uniprot.org/core/date"2001"xsd:gYear