en
Scientific article
Meta-analysis
English

Refinement of the X-linked nonsyndromic high-grade myopia locus MYP1 on Xq28 and exclusion of 13 known positional candidate genes by direct sequencing

Published inInvestigative ophthalmology & visual science, vol. 52, no. 9, p. 6814-6819
Publication date2011
Abstract

Myopia is a common vision problem affecting almost one third of the world's population. It can occur as an isolated genetic condition or be associated with other anomalies and/or syndromes. Seventeen myopia loci have been identified on various chromosomes; however, no specific gene mutations have yet been identified.

Keywords
  • Asian Continental Ancestry Group/genetics
  • Child
  • Child, Preschool
  • Chromosome Mapping
  • Chromosomes, Human, X/genetics
  • DNA Mutational Analysis
  • Female
  • Genes, Dominant/genetics
  • Genetic Association Studies/methods
  • Genetic Diseases, X-Linked/diagnosis/genetics
  • Genetic Linkage
  • Haplotypes
  • Humans
  • India/epidemiology
  • Lod Score
  • Male
  • Microsatellite Repeats
  • Myopia/diagnosis/genetics
  • Pedigree
Citation (ISO format)
RATNAMALA, Uppala et al. Refinement of the X-linked nonsyndromic high-grade myopia locus MYP1 on Xq28 and exclusion of 13 known positional candidate genes by direct sequencing. In: Investigative ophthalmology & visual science, 2011, vol. 52, n° 9, p. 6814–6819. doi: 10.1167/iovs.10-6815
Main files (1)
Article (Published version)
accessLevelRestricted
Identifiers
ISSN of the journal0146-0404
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