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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
by
Jones, Amy V
,
Curtiss, Darin
,
Harris, Claire
,
Southerington, Tom
,
Hautalahti, Marco
,
Wihuri, Pauli
,
Mäkelä, Johanna
,
Kallionpää, Roosa E
,
Makkonen, Enni
,
Knopp, Theresa
,
Mannermaa, Arto
,
Mäkinen, Erna
,
Moilanen, Anne-Mari
,
Tezel, Tongalp H
,
Waheed, Nadia K
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