Small intragenic deletion in FOXP2 associated with childhood apraxia of speech and dysarthria

No abstract is available for this paper.

• Publication year

  2013

• Venue

  American Journal of Medical Genetics. Part A

• Publication date

  2013-09-01

• Fields of study

  Medicine

• Identifiers
  DOI 10.1002/ajmg.a.36055PMID 23918746
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

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