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Genetic Candidate Variants in Two Multigenerational Families with Childhood Apraxia of Speech

Childhood apraxia of speech (CAS) is a severe and socially debilitating form of speech sound disorder with suspected genetic involvement, but the genetic etiology is not yet well understood. Very few known or putative causal genes have been identified to date, e.g., FOXP2 and BCL11A. Building a know...

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Detalhes bibliográficos
Publicado no:PLoS One
Main Authors: Peter, Beate, Wijsman, Ellen M., Nato, Alejandro Q., Matsushita, Mark M., Chapman, Kathy L., Stanaway, Ian B., Wolff, John, Oda, Kaori, Gabo, Virginia B., Raskind, Wendy H.
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2016
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4847873/
https://ncbi.nlm.nih.gov/pubmed/27120335
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0153864
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