{"created":"2023-06-23T12:21:12.663043+00:00","id":12761,"links":{},"metadata":{"_buckets":{"deposit":"a3394ba9-9aa2-4ea7-8bec-99923a8e9207"},"_deposit":{"created_by":19,"id":"12761","owners":[19],"pid":{"revision_id":0,"type":"depid","value":"12761"},"status":"published"},"_oai":{"id":"oai:asahi-u.repo.nii.ac.jp:00012761","sets":["64:123"]},"author_link":["15902"],"item_10_creator_30":{"attribute_name":"教員氏名","attribute_type":"creator","attribute_value_mlt":[{"creatorNames":[{"creatorName":"松原, 誠"}],"nameIdentifiers":[{"nameIdentifier":"15902","nameIdentifierScheme":"WEKO"}]}]},"item_10_date_36":{"attribute_name":"発行又は発表の年月","attribute_value_mlt":[{"subitem_date_issued_datetime":"2019-11"}]},"item_10_textarea_29":{"attribute_name":"業績分類","attribute_value_mlt":[{"subitem_textarea_value":"学会発表"}]},"item_10_textarea_31":{"attribute_name":"発行、発表雑誌等、又は発表学会等の名称","attribute_value_mlt":[{"subitem_textarea_value":"第36回日本障害者歯科学会総会および学術大会"}]},"item_10_textarea_35":{"attribute_name":"単著、共著の別","attribute_value_mlt":[{"subitem_textarea_value":"共同"}]},"item_10_textarea_42":{"attribute_name":"概要","attribute_value_mlt":[{"subitem_textarea_value":"OXG1遺伝子は2008年に新たに発見された非典型的Rett症候群（以下RTT）の関連遺伝子である．生後早期から重度の発達遅滞がみられ非典型的RTTの先天型に分類される．FOXG1遺伝子の変異はRTTの中でも症例数が少なく，比較が難しいため口腔内所見をまとめるとともに，これまで報告されている典型RTT，非典型RTTの口腔内所見と比較し，今後の患児の検討を行なった"}]},"item_access_right":{"attribute_name":"アクセス権","attribute_value_mlt":[{"subitem_access_right":"metadata only access","subitem_access_right_uri":"http://purl.org/coar/access_right/c_14cb"}]},"item_language":{"attribute_name":"言語","attribute_value_mlt":[{"subitem_language":"jpn"}]},"item_resource_type":{"attribute_name":"資源タイプ","attribute_value_mlt":[{"resourcetype":"other","resourceuri":"http://purl.org/coar/resource_type/c_1843"}]},"item_title":"FOXG1遺伝子に変異がみられた非典型的Rett症候群患児の口腔内所","item_titles":{"attribute_name":"タイトル","attribute_value_mlt":[{"subitem_title":"FOXG1遺伝子に変異がみられた非典型的Rett症候群患児の口腔内所"}]},"item_type_id":"10","owner":"19","path":["123"],"pubdate":{"attribute_name":"公開日","attribute_value":"2020-10-23"},"publish_date":"2020-10-23","publish_status":"0","recid":"12761","relation_version_is_last":true,"title":["FOXG1遺伝子に変異がみられた非典型的Rett症候群患児の口腔内所"],"weko_creator_id":"19","weko_shared_id":-1},"updated":"2023-06-23T13:00:37.855813+00:00"}