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Paper Details

A rare penetrant mutation in CFH confers high risk of age-related macular degeneration.
Nat Genet
247
2011
AMD, C, CFH, R1210C, Y402H, age-related macular degeneration, atypical hemolytic uremic syndrome, c.1204C, c.1204C>T, c.3628C, c.3628C>T, complex disease, gene encoding complement factor H, intronic rs1410996 SNP, rs1061170, rs1410996, susceptibility alleles
Author NameAffiliation
Soumya RaychaudhuriBrigham and Women's Hospital
Soumya RaychaudhuriBrigham and Women's Hospital
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