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Title

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

Authors
Ratnamala, Uppala
Rawal, Rakesh
Singh, Raminder
Vishnupriya, Satti
Himabindu, Pamini
Rao, Vittal
Aggarwal, Somesh
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Published in Investigative Ophthalmology & Visual Science. 2011, vol. 52, no. 9, p. 6814-9
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/geneticsChildChild, PreschoolChromosome MappingChromosomes, Human, X/geneticsDNA Mutational AnalysisFemaleGenes, Dominant/geneticsGenetic Association Studies/methodsGenetic Diseases, X-Linked/diagnosis/geneticsGenetic LinkageHaplotypesHumansIndia/epidemiologyLod ScoreMaleMicrosatellite RepeatsMyopia/diagnosis/geneticsPedigree
Identifiers
PMID: 21357393
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Structures
Research groups Groupe Giacobino Ariane (génétique) (923)
Pathologie Moléculaire de la Trisomie 21 et le Génome Humain (248)
Citation
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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. 6814-9. https://archive-ouverte.unige.ch/unige:25377

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Deposited on : 2013-01-11

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