JAG1 mutations are found in approximately one third of patients presenting with only one or two clinical features of Alagille syndrome

No abstract is available for this paper.

• Publication year

  2012

• Venue

  Clinical Genetics

• Publication date

  2012-07-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1111/j.1399-0004.2011.01749.xPMID 21752016
• 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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