Phenotyping and genotyping inherited retinal diseases: Molecular genetics, clinical and imaging features, and therapeutics of macular dystrophies, cone and cone-rod dystrophies, rod-cone dystrophies, Leber congenital amaurosis, and cone dysfunction syndromes-Reference-Cited by-同舟云学术

Phenotyping and genotyping inherited retinal diseases: Molecular genetics, clinical and imaging features, and therapeutics of macular dystrophies, cone and cone-rod dystrophies, rod-cone dystrophies, Leber congenital amaurosis, and cone dysfunction syndromes

Published:2024-05 Issue: Volume:100 Page:101244
ISSN:1350-9462
Container-title:Progress in Retinal and Eye Research
language:en
Short-container-title:Progress in Retinal and Eye Research

Author:

Georgiou Michalis,Robson Anthony G.,Fujinami Kaoru,de Guimarães Thales A.C.,Fujinami-Yokokawa Yu,Daich Varela Malena,Pontikos Nikolas,Kalitzeos Angelos,Mahroo Omar A.,Webster Andrew R.,Michaelides Michel

Funder

NIHR Biomedical Research Centre, Royal Marsden NHS Foundation Trust/Institute of Cancer Research

Moorfields Eye Hospital NHS Foundation Trust

Retina UK

Moorfields Eye Charity

Fight for Sight UK

UCL Institute of Ophthalmology, University College London

Macular Society

Alexander S. Onassis Public Benefit Foundation

Foundation Fighting Blindness

Wellcome Trust

A.G. Leventis Foundation