Functional analyses of rare genetic variants in complement component C9 identified in patients with age-related macular degeneration

Authors :: Kremlitzka, Mariann
Geerlings, M.J.
Jong, S. de
Bakker, B.
Nilsson, Sara C.
Fauser, Sascha
Hoyng, C.B.
Hollander, A.I. den
Blom, Anna M.
Kremlitzka, Mariann
Geerlings, M.J.
Jong, S. de
Bakker, B.
Nilsson, Sara C.
Fauser, Sascha
Hoyng, C.B.
Hollander, A.I. den
Blom, Anna M.
Source :: Human Molecular Genetics; 2678; 2688; 0964-6906; 27; ~Human Molecular Genetics~2678~2688~~~0964-6906~~27~~
Publication Year :: 2018
Abstract: Item does not contain fulltext

Database :: OAIster
Journal :: Human Molecular Genetics; 2678; 2688; 0964-6906; 27; ~Human Molecular Genetics~2678~2688~~~0964-6906~~27~~
Publication Type :: Electronic Resource
Accession number :: edsoai.on1284169163
Document Type :: Electronic Resource

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