Diagnostic challenges in a severely delayed infant with hypersomnolence, failure to thrive and arteriopathy: A unique case of γ‐hydroxybutyric aciduria and Williams syndrome

No abstract is available for this paper.

• Publication year

  2007

• Venue

  American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

• Publication date

  2007-10-05

• Fields of study

  Medicine

• Identifiers
  DOI 10.1002/ajmg.b.30553PMID 17471494
• 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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