A highly penetrant form of childhood apraxia of speech due to deletion of 16p11.2
- PMID: 26763793
- PMCID: PMC4717201
- DOI: 10.1038/ejhg.2015.230
A highly penetrant form of childhood apraxia of speech due to deletion of 16p11.2
Erratum for
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A highly penetrant form of childhood apraxia of speech due to deletion of 16p11.2.Eur J Hum Genet. 2016 Feb;24(2):302-6. doi: 10.1038/ejhg.2015.149. Epub 2015 Jul 15. Eur J Hum Genet. 2016. PMID: 26173965 Free PMC article.
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