Complete loss of function of the ubiquitin ligase HERC2 causes a severe neurodevelopmental phenotype

No abstract is available for this paper.

• Publication year

  2016

• Venue

  European Journal of Human Genetics

• Publication date

  2016-10-19

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1038/ejhg.2016.139PMID 27759030PMCID PMC5159772
• 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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