{"created":"2023-07-27T06:38:31.686225+00:00","id":26623,"links":{},"metadata":{"_buckets":{"deposit":"ea2dc6b5-a0eb-4f60-b321-5b883888a85e"},"_deposit":{"created_by":3,"id":"26623","owners":[3],"pid":{"revision_id":0,"type":"depid","value":"26623"},"status":"published"},"_oai":{"id":"oai:kanazawa-u.repo.nii.ac.jp:00026623","sets":["1761:1762:1763"]},"author_link":["44696","44699","44700","44697","210","44698"],"item_4_biblio_info_8":{"attribute_name":"書誌情報","attribute_value_mlt":[{"bibliographicIssueDates":{"bibliographicIssueDate":"2007-09-15","bibliographicIssueDateType":"Issued"},"bibliographicIssueNumber":"1-2","bibliographicPageEnd":"239","bibliographicPageStart":"236","bibliographicVolumeNumber":"260","bibliographic_titles":[{"bibliographic_title":"Journal of the Neurological Sciences"}]}]},"item_4_description_21":{"attribute_name":"抄録","attribute_value_mlt":[{"subitem_description":"A family with familial amyloid polyneuropathy (FAP) due to a transthyretin (TTR) Leu58Arg mutation was investigated clinicopathologically. The proband presented with sensorimotor-autonomic polyneuropathy and autopsy demonstrated massive amyloid deposition in the peripheral nerves and heart. However, the mother was characterized by carpal tunnel syndrome and ocular vitreous opacities. Thus, there was considerable phenotypic heterogeneity among family members despite the identical TTR genotype. © 2007 Elsevier B.V. All rights reserved.","subitem_description_type":"Abstract"}]},"item_4_description_5":{"attribute_name":"提供者所属","attribute_value_mlt":[{"subitem_description":"金沢大学医学部附属病院神経内科","subitem_description_type":"Other"}]},"item_4_publisher_17":{"attribute_name":"出版者","attribute_value_mlt":[{"subitem_publisher":"Elsevier"}]},"item_4_relation_12":{"attribute_name":"DOI","attribute_value_mlt":[{"subitem_relation_type":"isVersionOf","subitem_relation_type_id":{"subitem_relation_type_id_text":"10.1016/j.jns.2007.03.021","subitem_relation_type_select":"DOI"}}]},"item_4_source_id_9":{"attribute_name":"ISSN","attribute_value_mlt":[{"subitem_source_identifier":"0022-510X","subitem_source_identifier_type":"ISSN"}]},"item_4_version_type_25":{"attribute_name":"著者版フラグ","attribute_value_mlt":[{"subitem_version_resource":"http://purl.org/coar/version/c_ab4af688f83e57aa","subitem_version_type":"AM"}]},"item_creator":{"attribute_name":"著者","attribute_type":"creator","attribute_value_mlt":[{"creatorNames":[{"creatorName":"Motozaki, Yuko"}],"nameIdentifiers":[{}]},{"creatorNames":[{"creatorName":"Sugiyama, Yu"}],"nameIdentifiers":[{}]},{"creatorNames":[{"creatorName":"Ishida, Chiho"}],"nameIdentifiers":[{}]},{"creatorNames":[{"creatorName":"Komai, Kiyonobu"}],"nameIdentifiers":[{}]},{"creatorNames":[{"creatorName":"Matsubara, Shiro"}],"nameIdentifiers":[{},{}]},{"creatorNames":[{"creatorName":"Yamada, Masahito"}],"nameIdentifiers":[{},{},{},{}]}]},"item_files":{"attribute_name":"ファイル情報","attribute_type":"file","attribute_value_mlt":[{"accessrole":"open_date","date":[{"dateType":"Available","dateValue":"2017-10-05"}],"displaytype":"detail","filename":"HO-PR-MOTOZAKI-Y-236.pdf","filesize":[{"value":"257.6 kB"}],"format":"application/pdf","licensetype":"license_note","mimetype":"application/pdf","url":{"label":"HO-PR-MOTOZAKI-Y-236.pdf","url":"https://kanazawa-u.repo.nii.ac.jp/record/26623/files/HO-PR-MOTOZAKI-Y-236.pdf"},"version_id":"8977e151-2e3d-40e5-9a92-412fa501e9da"}]},"item_language":{"attribute_name":"言語","attribute_value_mlt":[{"subitem_language":"eng"}]},"item_resource_type":{"attribute_name":"資源タイプ","attribute_value_mlt":[{"resourcetype":"journal article","resourceuri":"http://purl.org/coar/resource_type/c_6501"}]},"item_title":"Phenotypic heterogeneity in a family with FAP due to a TTR Leu58Arg mutation: A clinicopathologic study","item_titles":{"attribute_name":"タイトル","attribute_value_mlt":[{"subitem_title":"Phenotypic heterogeneity in a family with FAP due to a TTR Leu58Arg mutation: A clinicopathologic study"}]},"item_type_id":"4","owner":"3","path":["1763"],"pubdate":{"attribute_name":"公開日","attribute_value":"2017-10-05"},"publish_date":"2017-10-05","publish_status":"0","recid":"26623","relation_version_is_last":true,"title":["Phenotypic heterogeneity in a family with FAP due to a TTR Leu58Arg mutation: A clinicopathologic study"],"weko_creator_id":"3","weko_shared_id":3},"updated":"2023-07-27T16:52:50.408683+00:00"}