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Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech
BACKGROUND: Childhood apraxia of speech (CAS) is a rare, severe, persistent pediatric motor speech disorder with associated deficits in sensorimotor, cognitive, language, learning and affective processes. Among other neurogenetic origins, CAS is the disorder segregating with a mutation in FOXP2 in a...
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| Main Authors: | , , , , , , , , |
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| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
BioMed Central
2013
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| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3851280/ https://ncbi.nlm.nih.gov/pubmed/24083349 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1866-1955-5-29 |
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