A common haplotype in the complement regulatory gene factor H (HF1/CFH) predisposes individuals to age-related macular degeneration.
Data(s) |
17/05/2005
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Identificador |
http://dx.doi.org/10.1073/pnas.0501536102 http://www.scopus.com/inward/record.url?scp=21044453724&partnerID=8YFLogxK |
Idioma(s) |
eng |
Direitos |
info:eu-repo/semantics/restrictedAccess |
Fonte |
Silvestri , G , Hageman , G S , Allikmets , R , Anderson , D H , Johnson , L V , Hancox , L S , Taiber , A J , Hardisty , L I , Hageman , J L , Stockman , H A , Borchardt , J D , Gehrs , K M , Smith , R J H , Russell , S R , Klaver , C C W , Barbazetto , I , Chang , S , Yannuzzi , L A , Barile , G R , Merriam , J C , Smith , R T , Olsh , A K , Bergeron , J , Zernant , J , Merriam , J E , Gold , B & Dean , M 2005 , ' A common haplotype in the complement regulatory gene factor H (HF1/CFH) predisposes individuals to age-related macular degeneration. ' Proceedings of the National Academy of Sciences , vol 102(20) , no. 20 , pp. 7227-7232 . DOI: 10.1073/pnas.0501536102 |
Palavras-Chave | #/dk/atira/pure/subjectarea/asjc/1300/1311 #Genetics #/dk/atira/pure/subjectarea/asjc/1000 #General |
Tipo |
article |