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http://purl.uniprot.org/citations/14635105http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/14635105http://www.w3.org/2000/01/rdf-schema#comment"Menkes disease (MD) is an X-linked multisystemic lethal disorder of copper metabolism dominated by neurodegenerative symptoms and connective tissue disturbances. MD results from mutations in the ATP7A gene, which encodes a membrane-bound copper transporting P-type ATPase located in the trans-Golgi network. In this study we describe screening of 383 unrelated patients affected with Menkes disease for gross deletions in ATP7A gene and finding of 57 patients. The present data suggests that gross deletion of ATP7A is the disease-causing mutation in 14.9% of the Menkes disease patients. Except for a few cases, gross gene deletions result in the classical form of Menkes disease with death in early childhood."xsd:string
http://purl.uniprot.org/citations/14635105http://purl.org/dc/terms/identifier"doi:10.1002/humu.10287"xsd:string
http://purl.uniprot.org/citations/14635105http://purl.uniprot.org/core/author"Horn N."xsd:string
http://purl.uniprot.org/citations/14635105http://purl.uniprot.org/core/author"Tumer Z."xsd:string
http://purl.uniprot.org/citations/14635105http://purl.uniprot.org/core/author"Birk Moller L."xsd:string
http://purl.uniprot.org/citations/14635105http://purl.uniprot.org/core/date"2003"xsd:gYear
http://purl.uniprot.org/citations/14635105http://purl.uniprot.org/core/name"Hum Mutat"xsd:string
http://purl.uniprot.org/citations/14635105http://purl.uniprot.org/core/pages"457-464"xsd:string
http://purl.uniprot.org/citations/14635105http://purl.uniprot.org/core/title"Screening of 383 unrelated patients affected with Menkes disease and finding of 57 gross deletions in ATP7A."xsd:string
http://purl.uniprot.org/citations/14635105http://purl.uniprot.org/core/volume"22"xsd:string
http://purl.uniprot.org/citations/14635105http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/14635105
http://purl.uniprot.org/citations/14635105http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/14635105
http://purl.uniprot.org/uniprot/#_B4DRW0-mappedCitation-14635105http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/14635105
http://purl.uniprot.org/uniprot/#_Q04656-mappedCitation-14635105http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/14635105
http://purl.uniprot.org/uniprot/#_Q762B6-mappedCitation-14635105http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/14635105
http://purl.uniprot.org/uniprot/#_Q59HD1-mappedCitation-14635105http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/14635105
http://purl.uniprot.org/uniprot/Q04656http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/14635105
http://purl.uniprot.org/uniprot/Q59HD1http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/14635105
http://purl.uniprot.org/uniprot/Q762B6http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/14635105
http://purl.uniprot.org/uniprot/B4DRW0http://purl.uniprot.org/core/mappedCitationhttp://purl.uniprot.org/citations/14635105