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All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year AND OR AND NOT All fields Title Creator / Publisher Keyword Year Sort by creator [A → Z]' creator [Z → A]' publishing year ↑ (asc)' publishing year ↓ (desc)' title [A → Z]' title [Z → A]' Simple Search Hits 1 – 1 of 1 1 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. - : BlackWell Publishing Ltd, 2015 Abstract: 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. Keyword: Case Reports URL: https://doi.org/10.1002/ccr3.167 http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4352365 BASE Hide details

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