Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech

BACKGROUND: Childhood apraxia of speech (CAS) is a rare, severe, persistent pediatric motor speech disorder with associated deficits in sensorimotor, cognitive, language, learning and affective processes. Among other neurogenetic origins, CAS is the disorder segregating with a mutation in FOXP2 in a...

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Detalhes bibliográficos
Main Authors: Worthey, Elizabeth A, Raca, Gordana, Laffin, Jennifer J, Wilk, Brandon M, Harris, Jeremy M, Jakielski, Kathy J, Dimmock, David P, Strand, Edythe A, Shriberg, Lawrence D
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2013
Assuntos:
Research
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3851280/
https://ncbi.nlm.nih.gov/pubmed/24083349
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1866-1955-5-29
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