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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4847873/ https://www.ncbi.nlm.nih.gov/pubmed/27120335 http://dx.doi.org/10.1371/journal.pone.0153864 |