Ten new cases further delineate the syndromic intellectual disability phenotype caused by mutations in DYRK1A

No abstract is available for this paper.

• Publication year

  2015

• Venue

  European Journal of Human Genetics

• Publication date

  2015-04-29

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1038/ejhg.2015.29PMID 25920557PMCID PMC4613470
• 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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