Heritability and genome-wide association study to assess genetic differences between advanced age-related macular degeneration subtypes.

Sobrin L, Ripke S, Yu Y, Fagerness J, Bhangale TR, Tan PL, Souied EH, Buitendijk GH, Merriam JE, Richardson AJ, Raychaudhuri S, Reynolds R, Chin KA, Lee AY, Leveziel N, Zack DJ, Campochiaro P, Smith RT, Barile GR, Hogg RE, Chakravarthy U, Behrens TW, Uitterlinden AG, van Duijn CM, Vingerling JR, Brantley MA, Baird PN, Klaver CC, Allikmets R, Katsanis N, Graham RR, Ioannidis JP, Daly MJ, Seddon JM
Ophthalmology. 2012 119 (9): 1874-85

PMID: 22705344 · PMCID: PMC3899891 · DOI:10.1016/j.ophtha.2012.03.014

MeSH Terms (15)

Choroidal Neovascularization Female Genetic Predisposition to Disease Genome-Wide Association Study Genotype Geographic Atrophy High-Temperature Requirement A Serine Peptidase 1 Humans Macular Degeneration Male Polymorphism, Single Nucleotide Proteins Risk Factors Serine Endopeptidases Siblings

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