Genome-wide association studies reveal genetic variants in CTNND2 for high myopia in Singapore Chinese.

No abstract is available for this paper.

• Publication year

  2011

• Venue

  Ophthalmology (Rochester, Minn.)

• Publication date

  2011-02-01

• Fields of study

  Medicine

• Identifiers
  DOI 10.1016/j.ophtha.2010.06.016PMID 21095009PMCID PMC3052933
• 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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