Large deletions of the KCNV2 gene are common in patients with cone dystrophy with supernormal rod response

No abstract is available for this paper.

• Publication year

  2011

• Venue

  Human Mutation

• Publication date

  2011-12-01

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1002/humu.21580PMID 21882291
• 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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