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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

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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