A highly penetrant form of childhood apraxia of speech due to deletion of 16p11.2

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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Main Authors: Fedorenko, Evelina (Author), Morgan, Angela (Author), Murray, Elizabeth (Author), Mei, Cristina (Author), Tager-Flusberg, Helen (Author), Fisher, Simon E (Author), Cardinaux, Anne (Contributor), Kanwisher, Nancy (Contributor)
Other Authors: Massachusetts Institute of Technology. Department of Brain and Cognitive Sciences (Contributor), McGovern Institute for Brain Research at MIT (Contributor)
Format: Article
Language:English
Published: Nature Publishing Group, 2018-01-08T18:42:15Z.
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