Refinement of the X-linked nonsyndromic high-grade myopia locus MYP1 on Xq28 and exclusion of 13 known positional candidate genes by direct sequencing
ContributorsRatnamala, Uppala; Lyle, Robert; Rawal, Rakesh; Singh, Raminder; Vishnupriya, Satti; Himabindu, Pamini; Rao, Vittal; Aggarwal, Somesh; Paluru, Prasuna; Bartoloni Riotto, Lucia; Young, Terri L; Giacobino, Ariane; Morris, Michael Andréw; Nath, Swapan K; Antonarakis, Stylianos; Radhakrishna, Uppala
Published inInvestigative ophthalmology & visual science, vol. 52, no. 9, p. 6814-6819
Publication date2011
Abstract
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)
Identifiers
- PID : unige:25377
- DOI : 10.1167/iovs.10-6815
- PMID : 21357393
ISSN of the journal0146-0404