Severe speech impairment is a distinguishing feature of FOXP1-related disorder
FOXP1-related disorder is characterized by a complex speech and language phenotype with prominent dysarthria, broader motor…
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FOXP1-related disorder is characterized by a complex speech and language phenotype with prominent dysarthria, broader motor…
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Our paper on Automatic speech recognition in neurodegenerative disease was recently published in International Journal of…
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Published in the European Journal of Human Genetics we expand the linguistic phenotype associated with SETBP1…
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Hardware selection is an important and often overlooked component of speech research. All data are acquired…
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Objective: To determine whether specific speech, language and oromotor profiles are associated with different patterns of polymicrogyria…
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Highlights • Four children with heterozygous WAC pathogenic variants and epilepsy are described. • All children had global…
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