Identification of a prevalent founder mutation in an Israeli Muslim Arab village confirms the role of PRCD in the aetiology of retinitis pigmentosa in humans

No abstract is available for this paper.

• Publication year

  2010

• Venue

  Journal of Medical Genetics

• Publication date

  2010-05-27

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1136/jmg.2009.073619PMID 20507925
• 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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