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...
প্রধান লেখক: | 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 |
---|---|
বিন্যাস: | Journal article |
ভাষা: | English |
প্রকাশিত: |
Elsevier
2019
|
অনুরূপ উপাদানগুলি
-
Novel homozygous splicing mutations in ARL2BP cause autosomal recessive retinitis pigmentosa
অনুযায়ী: Fiorentino, A, অন্যান্য
প্রকাশিত: (2018) -
Haplotypes in the complement factor H (CFH) gene: associations with drusen and advanced age-related macular degeneration.
অনুযায়ী: Peter J Francis, অন্যান্য
প্রকাশিত: (2007-11-01) -
CFH Y402H Confers Similar Risk of Soft Drusen and Both Forms of Advanced AMD.
প্রকাশিত: (2005-11-01) -
CFH Y402H confers similar risk of soft drusen and both forms of advanced AMD.
অনুযায়ী: Kristinn P Magnusson, অন্যান্য
প্রকাশিত: (2006-01-01) -
Phenogenon: Gene to phenotype associations for rare genetic diseases.
অনুযায়ী: Nikolas Pontikos, অন্যান্য
প্রকাশিত: (2020-01-01)