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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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| Publicado no: | PLoS One |
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| Main Authors: | , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Public Library of Science
2016
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| Assuntos: | |
| 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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