GPT2 mutations in autosomal recessive developmental disability: extending the clinical phenotype and population prevalence estimates

No abstract is available for this paper.

• Publication year

  2019

• Venue

  Human Genetics

• Publication date

  2019-08-30

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1007/s00439-019-02057-xPMID 31471722PMCID PMC6748651
• 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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