Crumbs homolog 1 (CRB1) mutations result in a thick human retina with abnormal lamination-Reference-Cited by-同舟云学术

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Crumbs homolog 1 (CRB1) mutations result in a thick human retina with abnormal lamination

Published:2003-05-01 Issue:9 Volume:12 Page:1073-1078
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:
Short-container-title:

Author:

Jacobson S. G.

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/12/9/1073/1755000/ddg117.pdf

Cited by 204 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Perturbed cell cycle phase-dependent positioning and nuclear migration of retinal progenitors along the apico-basal axis underlie global retinal disorganization in the LCA8-like mouse model;Developmental Biology;2024-09

2. Characteristics of Eyes With CRB1-Associated EOSRD/LCA: Age-Related Changes;American Journal of Ophthalmology;2024-07

3. In Silico CRISPR-Cas-Mediated Base Editing Strategies for Early-Onset, Severe Cone–Rod Retinal Degeneration in Three Crumbs homolog 1 Patients, including the Novel Variant c.2833G>A;Genes;2024-05-15

4. 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;Progress in Retinal and Eye Research;2024-05

5. Retinal Imaging Findings in Inherited Retinal Diseases;Journal of Clinical Medicine;2024-04-03

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