{"created":"2021-03-01T07:16:05.340724+00:00","id":37020,"links":{},"metadata":{"_buckets":{"deposit":"33b8ddc2-3487-4f6f-8e6e-d44a4d916834"},"_deposit":{"id":"37020","owners":[],"pid":{"revision_id":0,"type":"depid","value":"37020"},"status":"published"},"_oai":{"id":"oai:tsukuba.repo.nii.ac.jp:00037020","sets":["2780:938","3:62:5298:4904"]},"item_5_biblio_info_6":{"attribute_name":"書誌情報","attribute_value_mlt":[{"bibliographicIssueDates":{"bibliographicIssueDate":"2015-02","bibliographicIssueDateType":"Issued"},"bibliographicIssueNumber":"2","bibliographicPageEnd":"113","bibliographicPageStart":"110","bibliographicVolumeNumber":"3","bibliographic_titles":[{"bibliographic_title":"Clinical Case Reports"}]}]},"item_5_creator_3":{"attribute_name":"著者別名","attribute_type":"creator","attribute_value_mlt":[{"creatorNames":[{"creatorName":"野口, 惠美子"}],"nameIdentifiers":[{},{},{}]}]},"item_5_description_4":{"attribute_name":"抄録","attribute_value_mlt":[{"subitem_description":"The FOXP protein family (FOXP1-4) is a group of transcription factors that play important roles in embryological, immunological, hematological, and speech and language development. Here, we report FOXP1 de novo mutation and severe speech delay in an individual belonging to a non-Caucasian population.","subitem_description_type":"Abstract"}]},"item_5_publisher_27":{"attribute_name":"出版者","attribute_value_mlt":[{"subitem_publisher":"John Wiley & Sons Ltd."}]},"item_5_relation_10":{"attribute_name":"PubMed番号","attribute_value_mlt":[{"subitem_relation_type_id":{"subitem_relation_type_id_text":"25767709","subitem_relation_type_select":"PMID"}}]},"item_5_relation_11":{"attribute_name":"DOI","attribute_value_mlt":[{"subitem_relation_type_id":{"subitem_relation_type_id_text":"10.1002/ccr3.167","subitem_relation_type_select":"DOI"}}]},"item_5_rights_12":{"attribute_name":"権利","attribute_value_mlt":[{"subitem_rights":"© 2014 The Authors."},{"subitem_rights":"Clinical Case Reports published by John Wiley & Sons Ltd.  This is an open access article under the terms of the Creative Commons Attribution-NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes."}]},"item_5_select_15":{"attribute_name":"著者版フラグ","attribute_value_mlt":[{"subitem_select_item":"publisher"}]},"item_5_source_id_7":{"attribute_name":"ISSN","attribute_value_mlt":[{"subitem_source_identifier":"2050-0904","subitem_source_identifier_type":"ISSN"}]},"item_creator":{"attribute_name":"著者","attribute_type":"creator","attribute_value_mlt":[{"creatorNames":[{"creatorName":"Song, Hao"}],"nameIdentifiers":[{}]},{"creatorNames":[{"creatorName":"Makino, Yuka"}],"nameIdentifiers":[{}]},{"creatorNames":[{"creatorName":"Noguchi, Emiko"}],"nameIdentifiers":[{}]},{"creatorNames":[{"creatorName":"Arinami, Tadao"}],"nameIdentifiers":[{}]}]},"item_files":{"attribute_name":"ファイル情報","attribute_type":"file","attribute_value_mlt":[{"accessrole":"open_date","date":[{"dateType":"Available","dateValue":"2016-02-10"}],"displaytype":"detail","filename":"CCR_3-2.pdf","filesize":[{"value":"57.7 kB"}],"format":"application/pdf","licensetype":"license_9","mimetype":"application/pdf","url":{"label":"CCR_3-2","url":"https://tsukuba.repo.nii.ac.jp/record/37020/files/CCR_3-2.pdf"},"version_id":"c863a684-cd6b-4e98-a967-496e207ecff2"}]},"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":"A case report of de novo missense FOXP1 mutation in a non-Caucasian patient with global developmental delay and severe speech impairment","item_titles":{"attribute_name":"タイトル","attribute_value_mlt":[{"subitem_title":"A case report of de novo missense FOXP1 mutation in a non-Caucasian patient with global developmental delay and severe speech impairment"}]},"item_type_id":"5","owner":"1","path":["938","4904"],"pubdate":{"attribute_name":"公開日","attribute_value":"2016-02-10"},"publish_date":"2016-02-10","publish_status":"0","recid":"37020","relation_version_is_last":true,"title":["A case report of de novo missense FOXP1 mutation in a non-Caucasian patient with global developmental delay and severe speech impairment"],"weko_creator_id":"1","weko_shared_id":5},"updated":"2022-04-27T09:06:20.120520+00:00"}