Leber congenital amaurosis--genotyping required for possible inclusion in a clinical trial.

No abstract is available for this paper.

• Publication year

  2003

• Venue

  Advances in Experimental Medicine and Biology

• Publication date

  Unknown publication date

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1007/978-1-4615-0067-4_9PMID 15180249
• 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.

• Leber Congenital Amaurosis

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  1999cited by this paper
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• Crx, a novel otx-like homeobox gene, shows photoreceptor-specific expression and regulates photoreceptor differentiation.

  1997cited by this paper
• Mutations in RPE65 cause Leber's congenital amaurosis

  1997influential reference
• Retinal–specific guanylate cyclase gene mutations in Leber's congenital amaurosis

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