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A highly penetrant form of childhood apraxia of speech due to deletion of 16p11.2
Individuals with heterozygous 16p11.2 deletions reportedly suffer from a variety of difficulties with speech and language. Indeed, recent copy-number variant screens of children with childhood apraxia of speech (CAS), a specific and rare motor speech disorder, have identified three unrelated individ...
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| Publicado no: | Eur J Hum Genet |
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| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Nature Publishing Group
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4717199/ https://ncbi.nlm.nih.gov/pubmed/26173965 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2015.149 |
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