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http://purl.uniprot.org/citations/15851746http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/15851746http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/15851746http://www.w3.org/2000/01/rdf-schema#comment"Spinal and bulbar muscular atrophy (SBMA) is an X-linked, late-onset neuroendocrine disorder resulting from an expansion of a CAG repeat in the androgen receptor gene. Reported here is a detailed phenotypic study in a series of seven patients from the same family with SBMA with 50 to 54 CAG repeats, juvenile onset (mean age at onset 13 years [8 to 15 years]), and rapid progression leading to compromised ambulation in the mid-20s."xsd:string
http://purl.uniprot.org/citations/15851746http://purl.org/dc/terms/identifier"doi:10.1212/01.wnl.0000158617.41819.f3"xsd:string
http://purl.uniprot.org/citations/15851746http://purl.org/dc/terms/identifier"doi:10.1212/01.wnl.0000158617.41819.f3"xsd:string
http://purl.uniprot.org/citations/15851746http://purl.uniprot.org/core/author"Echaniz-Laguna A."xsd:string
http://purl.uniprot.org/citations/15851746http://purl.uniprot.org/core/author"Echaniz-Laguna A."xsd:string
http://purl.uniprot.org/citations/15851746http://purl.uniprot.org/core/author"Anheim M."xsd:string
http://purl.uniprot.org/citations/15851746http://purl.uniprot.org/core/author"Anheim M."xsd:string
http://purl.uniprot.org/citations/15851746http://purl.uniprot.org/core/author"Cossee M."xsd:string
http://purl.uniprot.org/citations/15851746http://purl.uniprot.org/core/author"Cossee M."xsd:string
http://purl.uniprot.org/citations/15851746http://purl.uniprot.org/core/author"Rousso E."xsd:string
http://purl.uniprot.org/citations/15851746http://purl.uniprot.org/core/author"Rousso E."xsd:string
http://purl.uniprot.org/citations/15851746http://purl.uniprot.org/core/author"Tranchant C."xsd:string
http://purl.uniprot.org/citations/15851746http://purl.uniprot.org/core/author"Tranchant C."xsd:string
http://purl.uniprot.org/citations/15851746http://purl.uniprot.org/core/date"2005"xsd:gYear
http://purl.uniprot.org/citations/15851746http://purl.uniprot.org/core/date"2005"xsd:gYear
http://purl.uniprot.org/citations/15851746http://purl.uniprot.org/core/name"Neurology"xsd:string
http://purl.uniprot.org/citations/15851746http://purl.uniprot.org/core/name"Neurology"xsd:string
http://purl.uniprot.org/citations/15851746http://purl.uniprot.org/core/pages"1458-1460"xsd:string
http://purl.uniprot.org/citations/15851746http://purl.uniprot.org/core/pages"1458-1460"xsd:string
http://purl.uniprot.org/citations/15851746http://purl.uniprot.org/core/title"A family with early-onset and rapidly progressive X-linked spinal and bulbar muscular atrophy."xsd:string
http://purl.uniprot.org/citations/15851746http://purl.uniprot.org/core/title"A family with early-onset and rapidly progressive X-linked spinal and bulbar muscular atrophy."xsd:string
http://purl.uniprot.org/citations/15851746http://purl.uniprot.org/core/volume"64"xsd:string
http://purl.uniprot.org/citations/15851746http://purl.uniprot.org/core/volume"64"xsd:string