Late-Onset Autosomal Dominant Macular Degeneration Caused by Deletion of the CRX Gene-Reference-Cited by-同舟云学术

Late-Onset Autosomal Dominant Macular Degeneration Caused by Deletion of the CRX Gene

Published:2023-01 Issue:1 Volume:130 Page:68-76
ISSN:0161-6420
Container-title:Ophthalmology
language:en
Short-container-title:Ophthalmology

Author:

Yahya Samar^ORCID,Smith Claire E.L.,Poulter James A.,McKibbin Martin,Arno Gavin^ORCID,Ellingford Jamie,Kämpjärvi Kati,Khan Muhammad I.,Cremers Frans P.M.,Hardcastle Alison J.,Castle Bruce,Steel David H.W.,Webster Andrew R.,Black Graeme C.,El-Asrag Mohammed E.,Ali Manir^ORCID,Toomes Carmel^ORCID,Inglehearn Chris F.,Ingram Stuart,Taylor Rachel,Manson Forbes,Sergouniotis Panagiotis,Pontikos Nikolas,Cheetham Michael,Fiorentino Alessia,Downes Susan,Yu Jing,Halford Stephanie,Broadgate Suzanne,van Heyningen Veronica,Ambrose John C.,Arumugam Prabhu,Bevers Roel,Bleda Marta,Boardman-Pretty Freya,Boustred Christopher R.,Brittain Helen,Caulfield Mark J.,Chan Georgia C.,Elgar Greg,Fowler Tom,Giess Adam,Hamblin Angela,Henderson Shirley,Hubbard Tim J.P.,Jackson Rob,Jones Louise J.,Kasperaviciute Dalia,Kayikci Melis,Kousathanas Athanasios,Lahnstein Lea,Leigh Sarah E.A.,Leong Ivonne U.S.,Lopez Javier F.,Maleady-Crowe Fiona,McEntagart Meriel,Minneci Federico,Moutsianas Loukas,Mueller Michael,Murugaesu Nirupa,Need Anna C.,O’Donovan Peter,Odhams Chris A.,Patch Christine,Pereira Mariana Buongermino,Perez-Gil Daniel,Pullinger John,Rahim Tahrima,Rendon Augusto,Rogers Tim,Savage Kevin,Sawant Kushmita,Scott Richard H.,Siddiq Afshan,Sieghart Alexander,Smith Samuel C.,Sosinsky Alona,Stuckey Alexander,Tanguy Mélanie,Taylor Tavares Ana Lisa,Thomas Ellen R.A.,Thompson Simon R.,Tucci Arianna,Welland Matthew J.,Williams Eleanor,Witkowska Katarzyna,Wood Suzanne M.

Publisher

Elsevier BV

Subject

Ophthalmology

Reference32 articles.

1. Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptor;Fruend;Cell,1997

2. Retinopathy and attenuated circadian entrainment in Crx-deficient mice;Furukawa;Nat Genet,1999

3. Genetic linkage of cone–rod retinal dystrophy to chromosome 19q and evidence for segregation distortion;Evans;Nat Genet,1994

4. Mutations in the cone-rod homeobox gene are associated with the cone-rod dystrophy photoreceptor degeneration;Swain;Neuron,1997

5. A range of clinical phenotypes associated with mutations in CRX, a photoreceptor transcription-factor gene;Sohocki;Am J Hum Genet,1998

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1. Clinical, Genetic and Histopathological Characteristics of CRX-associated Retinal Dystrophies;Ophthalmology Retina;2024-08

2. Towards Uncovering the Role of Incomplete Penetrance in Maculopathies through Sequencing of 105 Disease-Associated Genes;Biomolecules;2024-03-19

3. Transcriptional precision in photoreceptor development and diseases – Lessons from 25 years of CRX research;Frontiers in Cellular Neuroscience;2024-02-13

4. Occult Macular Dysfunction Syndrome: Identification of Multiple Pathologies in a Clinical Spectrum of Macular Dysfunction with Normal Fundus in East Asian Patients: EAOMD Report No. 5;Genes;2023-09-26

5. Genotypic Profile and Clinical Characteristics of CRX-Associated Retinopathy in Koreans;Genes;2023-05-08