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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Vydáno v:Eur J Hum Genet
Hlavní autoři: Fedorenko, Evelina, Morgan, Angela, Murray, Elizabeth, Cardinaux, Annie, Mei, Cristina, Tager-Flusberg, Helen, Fisher, Simon E, Kanwisher, Nancy
Médium: Artigo
Jazyk:Inglês
Vydáno: Nature Publishing Group 2016
Témata:
Short Report
On-line přístup: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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