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An assessment of prevalence of Type 1 CFI rare variants in ..:
Jones, Amy
;
Curtiss, Darin
;
Harris, Claire
...
10.1371/journal.pone.0272260. , 2023
Link:
http://hdl.handle.net/10138/352460
RT Journal T1
An assessment of prevalence of Type 1 CFI rare variants in European AMD, and why lack of broader genetic data hinders development of new treatments and healthcare access
UL https://suche.suub.uni-bremen.de/peid=base-ftunivhelsihelda:oai:helda.helsinki.fi:10138_352460&Exemplar=1&LAN=DE A1 Jones, Amy A1 Curtiss, Darin A1 Harris, Claire A1 Southerington, Tom A1 Hautalahti, Marco A1 Wihuri, Pauli A1 Mäkelä, Johanna A1 Kallionpää, Roosa E A1 Makkonen, Enni A1 Knopp, Theresa A1 Mannermaa, Arto A1 Mäkinen, Erna A1 Moilanen, Anne-Mari A1 Tezel, Tongalp H A1 Waheed, Nadia K PB PUBLIC LIBRARY OF SCIENCE YR 2023 K1 Genome-wide association K1 Macular degeneration K1 Factor-i K1 Complement-system K1 High-risk K1 Disease K1 C3b K1 Polymorphisms K1 Inactivator K1 Mutations K1 Biomedicine JF 10.1371/journal.pone.0272260 LK http://hdl.handle.net/10138/352460 DO http://hdl.handle.net/10138/352460 SF ELIB - SuUB Bremen
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