https://lupinepublishers.com/ophthalmology-journal/fulltext/keratoconus-and-cone-rod-dystrophy-among-brothers-clinical-case-study-and-genetic-analysis.ID.000133.php
Keratoconus and Cone-Rod Dystrophy among Brothers: Clinical Case Study and Genetic Analysis
Keratoconus is a multifactorial degenerative corneal disorder characterized by corneal thinning and ectasia, with most cases occurring sporadically. However,...
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https://herseninstituut.nl/publicaties/homozygosity-mapping-in-patients-with-cone-rod-dystrophy-novel-mutations-and-clinical-characterizations/
Homozygosity mapping in patients with cone-rod dystrophy: novel mutations and clinical...
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https://www.kokogenetics.com/en/results/pet-health-test/cone-rod-dystrophy-1
Cone-Rod Dystrophy 1 - Dog genetic disease testing
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https://boris-portal.unibe.ch/entities/publication/38ba0069-3652-4165-bc9f-714076770340
Mutations in CNNM4 cause recessive cone-rod dystrophy with amelogenesis imperfecta.
Cone-rod dystrophies are inherited dystrophies of the retina characterized by the accumulation of deposits mainly localized to the cone-rich macular region of...
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https://rarediseases.info.nih.gov/diseases/1462/x-linked-cone-rod-dystrophy-2
X-linked cone-rod dystrophy 2 | About the Disease | GARD
Find symptoms and other information about X-linked cone-rod dystrophy 2.
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https://aphconnectcenter.org/visionaware/eye-conditions/eye-conditions-associated-with-blindness-c/cone-rod-dystrophy/
Cone-Rod Dystrophy - APH ConnectCenter
Apr 6, 2026 - Learn about cone rod dystrophy, a group of inherited diseases that cause deterioration of the retina's light-sensitive cells. Understand its impact on vision...
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https://animalgenetics.com/dog-tests/canine-disorder-tests/24-Cord1/
Cone-Rod Dystrophy-PRA (cord1) - Animal Genetics
Oct 18, 2023 - Progressive Retinal Atrophy-Cone-Rod Dystrophy (crd1-PRA) Description Cord1-PRA or crd1-PRA is a type of Progressive Retinal Atrophy (PRA). PRA is a general...
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https://lkc.com/new/research/de-novo-variant-in-gucy2d-gene-causing-atypical-cone-rod-dystrophy-in-a-consanguineous-family-and-literature-review/
De novo variant in GUCY2D gene causing atypical cone-rod dystrophy in a consanguineous family and...
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https://omia.org/OMIA001455/9615/
OMIA:001455-9615: Retinal atrophy - Cone-rod dystrophy, NPHP4-related in Canis lupus familiaris...
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https://www.frontiersin.org/journals/molecular-neuroscience/articles/10.3389/fnmol.2014.00025/full
Frontiers | RNA interference gene therapy in dominant retinitis pigmentosa and cone-rod dystrophy...
RNA interference (RNAi) knockdown is an efficacious therapeutic strategy for silencing genes causative for dominant retinal dystrophies. To test this, we use...
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https://researchconnect.buffalo.edu/en/publications/rtn4ip1-associated-non-syndromic-optic-neuropathy-and-rod-cone-dy/
RTN4IP1-associated non-syndromic optic neuropathy and rod-cone dystrophy - SUNY University at...
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