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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: | , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
2012
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| Matèries: | |
| 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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