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Novel Candidate Genes and Regions for Childhood Apraxia of Speech (CAS) Identified by Array Comparative Genomic Hybridization

PURPOSE: The goal of this study was to identify new candidate genes and genomic copy number variations associated with a rare, severe, and persistent speech disorder termed Childhood Apraxia of Speech (CAS). CAS is the speech disorder segregating with a mutation in FOXP2 in a multigenerational Londo...

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Autors principals: Laffin, Jennifer J.S., Raca, Gordana, Jackson, Craig A., Strand, Edythe A., Jakielski, Kathy J., Shriberg, Lawrence D.
Format: Artigo
Idioma:Inglês
Publicat: 2012
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Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3563158/
https://ncbi.nlm.nih.gov/pubmed/22766611
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/gim.2012.72
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