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A case report of de novo missense FOXP1 mutation in a non-Caucasian patient with global developmental delay and severe speech impairment
http://hdl.handle.net/2241/00135068
http://hdl.handle.net/2241/0013506899bec0dd-d8c0-4e59-804a-f9b2b1853902
名前 / ファイル | ライセンス | アクション |
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CCR_3-2 (57.7 kB)
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Item type | Journal Article(1) | |||||
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公開日 | 2016-02-10 | |||||
タイトル | ||||||
タイトル | A case report of de novo missense FOXP1 mutation in a non-Caucasian patient with global developmental delay and severe speech impairment | |||||
言語 | ||||||
言語 | eng | |||||
資源タイプ | ||||||
資源 | http://purl.org/coar/resource_type/c_6501 | |||||
タイプ | journal article | |||||
著者 |
Song, Hao
× Song, Hao× Makino, Yuka× Noguchi, Emiko× Arinami, Tadao |
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著者別名 |
野口, 惠美子
× 野口, 惠美子 |
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抄録 | ||||||
内容記述タイプ | Abstract | |||||
内容記述 | 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. | |||||
書誌情報 |
Clinical Case Reports 巻 3, 号 2, p. 110-113, 発行日 2015-02 |
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ISSN | ||||||
収録物識別子タイプ | ISSN | |||||
収録物識別子 | 2050-0904 | |||||
PubMed番号 | ||||||
識別子タイプ | PMID | |||||
関連識別子 | 25767709 | |||||
DOI | ||||||
識別子タイプ | DOI | |||||
関連識別子 | 10.1002/ccr3.167 | |||||
権利 | ||||||
権利情報 | © 2014 The Authors. | |||||
権利 | ||||||
権利情報 | 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. | |||||
著者版フラグ | ||||||
値 | publisher | |||||
出版者 | ||||||
出版者 | John Wiley & Sons Ltd. |