Cell death triggered by a novel mutation in the alphaA-crystallin gene underlies autosomal dominant cataract linked to chromosome 21qMACKAY, Donna S; ANDLEY, Usha P; SHIELS, Alan et al.European journal of human genetics. 2003, Vol 11, Num 10, pp 784-793, issn 1018-4813, 10 p.Article

Association of Complement Factor H and LOC387715 Genotypes with Response of Exudative Age-Related Macular Degeneration to Intravitreal BevacizumabBRANTLEY, Milam A; FANG, Amy M; KING, Jennifer M et al.Ophthalmology (Rochester, MN). 2007, Vol 114, Num 12, pp 2168-2173, issn 0161-6420, 6 p.Article

A nonsense mutation in CRYBB1 associated with autosomal dominant cataract linked to human chromosome 22qMACKAY, Donna S; BOSKOVSKA, Olivera B; KNOPF, Harry L. S et al.American journal of human genetics. 2002, Vol 71, Num 5, pp 1216-1221, issn 0002-9297, 6 p.Article

CHMP4B, a novel gene for autosomal dominant cataracts linked to chromosome 20qSHIELS, Alan; BENNETT, Thomas M; KNOPF, Harry L. S et al.American journal of human genetics. 2007, Vol 81, Num 3, pp 596-606, issn 0002-9297, 11 p.Article