May 2021
Severe speech impairment is a distinguishing feature of FOXP1-related disorder
FOXP1-related disorder is characterized by prominent dysarthria, motor planning deficits, and phonological errors.
Read summary →Ruth O Braden, David J Amori, Simon E Fisher, Cristina Mei, Candace T Muers, Heather Mefford, Deepak Gill, Siddharth Srivastava, Lindsay C Swanson, Himanshu Goel, Ingrid E Scheffer, Angela T Morgan
FOXP1-related disorder is characterized by prominent dysarthria, motor planning deficits, and phonological errors.
Read summary →Ilse Meerschaut, Daniel Rochefort, Nicole Revencu, Justine Petre, Christina Corsello, Guy A Rouleau (2017)
Clinical and genetic data from 48 individuals with FOXP1 variants documenting intellectual disability, language impairment and neuromotor delay.
Read summary →Noriyoshi Usui, Daniel J Araujo, Ashwinikumar Kulkarni, Marissa Co, Jacob Ellegood, Matthew Harper, Kazuya Toriumi, Jason P Lerch, Genevieve Konopka
FOXP1 deletion in the neocortex affects neonatal vocalizations, cortical organisation, and neuron migration in mice.
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