| http://purl.uniprot.org/citations/28451781 | http://www.w3.org/1999/02/22-rdf-syntax-ns#type | http://purl.uniprot.org/core/Journal_Citation |
| http://purl.uniprot.org/citations/28451781 | http://www.w3.org/2000/01/rdf-schema#comment | "ATP7A is a copper-transporting P-type adenosine triphosphatase whose loss of function leads to the Menkes disease, an X-linked copper metabolism multi-organ disorder (1 in 100.000 births). Here we document our experience with the ATP7A linked diseases in Italy. We analyzed the exonic structure of the ATP7A gene in 25 unrelated Italian families and studied the variants of unknown significance. We identified 22 different DNA alterations, 13 of which first reported in this study. The classical Menkes phenotype was present in 21 of the 25 families and was linked with highly damaging mutations (7 nonsense; 4 frame-shift; 2 small in-frame deletions, 2 splice site alterations, 2 gross deletions, and 1 gross duplication). Of the 4 cases with milder variants of the Menkes disease two had a missense mutation, one a leaky splice site alteration and one a nonsense mutation in exon 22. We determined in silico that all the mutations leading to the classical Menkes disease leave no residual activity of ATP7A including the apparently less severe in-frame deletions. Whereas milder forms of the disease are characterized by mutations that allow a limited residual activity of ATP7A, including the nonsense mutation observed."xsd:string |
| http://purl.uniprot.org/citations/28451781 | http://purl.org/dc/terms/identifier | "doi:10.1007/s11011-017-0010-8"xsd:string |
| http://purl.uniprot.org/citations/28451781 | http://purl.uniprot.org/core/author | "Segat D."xsd:string |
| http://purl.uniprot.org/citations/28451781 | http://purl.uniprot.org/core/author | "de Gemmis P."xsd:string |
| http://purl.uniprot.org/citations/28451781 | http://purl.uniprot.org/core/author | "Lorenzetto E."xsd:string |
| http://purl.uniprot.org/citations/28451781 | http://purl.uniprot.org/core/author | "Enzo M.V."xsd:string |
| http://purl.uniprot.org/citations/28451781 | http://purl.uniprot.org/core/author | "Hladnik U."xsd:string |
| http://purl.uniprot.org/citations/28451781 | http://purl.uniprot.org/core/author | "Cattelan P."xsd:string |
| http://purl.uniprot.org/citations/28451781 | http://purl.uniprot.org/core/date | "2017"xsd:gYear |
| http://purl.uniprot.org/citations/28451781 | http://purl.uniprot.org/core/name | "Metab Brain Dis"xsd:string |
| http://purl.uniprot.org/citations/28451781 | http://purl.uniprot.org/core/pages | "1173-1183"xsd:string |
| http://purl.uniprot.org/citations/28451781 | http://purl.uniprot.org/core/title | "13 novel putative mutations in ATP7A found in a cohort of 25 Italian families."xsd:string |
| http://purl.uniprot.org/citations/28451781 | http://purl.uniprot.org/core/volume | "32"xsd:string |
| http://purl.uniprot.org/citations/28451781 | http://www.w3.org/2004/02/skos/core#exactMatch | http://purl.uniprot.org/pubmed/28451781 |
| http://purl.uniprot.org/citations/28451781 | http://xmlns.com/foaf/0.1/primaryTopicOf | https://pubmed.ncbi.nlm.nih.gov/28451781 |
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| http://purl.uniprot.org/uniprot/#_Q04656-mappedCitation-28451781 | http://www.w3.org/1999/02/22-rdf-syntax-ns#object | http://purl.uniprot.org/citations/28451781 |
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