Associated Papers
C-reactive protein and CFH, ARMS2/HTRA1 gene variants are independently associated with risk of macular degeneration.
Seddon JM et al.
Ophthalmology, 2010
The dot-and-fleck retinopathy of X linked Alport syndrome is independent of complement factor H (CFH) gene polymorphisms.
Liu J et al.
The British Journal of Ophthalmology, 2009
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