Loss-of-Function Mutations in the CFH Gene Affecting Alternatively Encoded Factor H-like 1 Protein Cause Dominant Early-Onset Macular Drusen.
Purpose To characterize the molecular mechanism underpinning early-onset macular drusen (EOMD), a phenotypically severe subtype of age-related macular degeneration (AMD), in a subgroup of patients. Design Multicenter case series, in vitro experimentation, and retrospective analysis of previously re...
Những tác giả chính: | Taylor, RL, Poulter, JA, Downes, SM, McKibbin, M, Khan, KN, Inglehearn, CF, Webster, AR, Hardcastle, AJ, Michaelides, M, Bishop, PN, Clark, SJ, Black, GC, United Kingdom Inherited Retinal Dystrophy Consortium, Halford, S |
---|---|
Định dạng: | Journal article |
Ngôn ngữ: | English |
Được phát hành: |
Elsevier
2019
|
Những quyển sách tương tự
-
Novel homozygous splicing mutations in ARL2BP cause autosomal recessive retinitis pigmentosa
Bằng: Fiorentino, A, et al.
Được phát hành: (2018) -
Haplotypes in the complement factor H (CFH) gene: associations with drusen and advanced age-related macular degeneration.
Bằng: Peter J Francis, et al.
Được phát hành: (2007-11-01) -
CFH Y402H Confers Similar Risk of Soft Drusen and Both Forms of Advanced AMD.
Được phát hành: (2005-11-01) -
CFH Y402H confers similar risk of soft drusen and both forms of advanced AMD.
Bằng: Kristinn P Magnusson, et al.
Được phát hành: (2006-01-01) -
Phenogenon: Gene to phenotype associations for rare genetic diseases.
Bằng: Nikolas Pontikos, et al.
Được phát hành: (2020-01-01)