A case report of de novo missense FOXP1 mutation in a non-Caucasian patient with global developmental delay and severe speech impairment

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...

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Detalles Bibliográficos
Autores principales: Song, Hao, Makino, Yuka, Noguchi, Emiko, Arinami, Tadao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BlackWell Publishing Ltd 2015
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4352365/
https://www.ncbi.nlm.nih.gov/pubmed/25767709
http://dx.doi.org/10.1002/ccr3.167
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author Song, Hao
Makino, Yuka
Noguchi, Emiko
Arinami, Tadao
author_facet Song, Hao
Makino, Yuka
Noguchi, Emiko
Arinami, Tadao
author_sort Song, Hao
collection PubMed
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.
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spelling pubmed-43523652015-03-12 A case report of de novo missense FOXP1 mutation in a non-Caucasian patient with global developmental delay and severe speech impairment Song, Hao Makino, Yuka Noguchi, Emiko Arinami, Tadao Clin Case Rep Case Reports 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. BlackWell Publishing Ltd 2015-02 2014-11-24 /pmc/articles/PMC4352365/ /pubmed/25767709 http://dx.doi.org/10.1002/ccr3.167 Text en © 2014 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. http://creativecommons.org/licenses/by-nc/4.0/ 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.
spellingShingle Case Reports
Song, Hao
Makino, Yuka
Noguchi, Emiko
Arinami, Tadao
A case report of de novo missense FOXP1 mutation in a non-Caucasian patient with global developmental delay and severe speech impairment
title A case report of de novo missense FOXP1 mutation in a non-Caucasian patient with global developmental delay and severe speech impairment
title_full A case report of de novo missense FOXP1 mutation in a non-Caucasian patient with global developmental delay and severe speech impairment
title_fullStr A case report of de novo missense FOXP1 mutation in a non-Caucasian patient with global developmental delay and severe speech impairment
title_full_unstemmed A case report of de novo missense FOXP1 mutation in a non-Caucasian patient with global developmental delay and severe speech impairment
title_short A case report of de novo missense FOXP1 mutation in a non-Caucasian patient with global developmental delay and severe speech impairment
title_sort case report of de novo missense foxp1 mutation in a non-caucasian patient with global developmental delay and severe speech impairment
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4352365/
https://www.ncbi.nlm.nih.gov/pubmed/25767709
http://dx.doi.org/10.1002/ccr3.167
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