Mutations in the CRB1 Gene Cause Leber Congenital Amaurosis-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Mutations in the CRB1 Gene Cause Leber Congenital Amaurosis

Published:2001-03-01 Issue:3 Volume:119 Page:415
ISSN:0003-9950
Container-title:Archives of Ophthalmology
language:en
Short-container-title:Arch Ophthalmol

Author:

Lotery Andrew J.

Publisher

American Medical Association (AMA)

Subject

Ophthalmology

Cited by 200 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. Progressive nyctalopia and tunnel vision in a young man;Clinical Cases in Medical Retina;2025

2. Congenital blindness and retinopathy in a young girl;Clinical Cases in Medical Retina;2025

3. 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

4. Human CRB1 and CRB2 form homo- and heteromeric protein complexes in the retina;Life Science Alliance;2024-04-03

5. Pigmented paravenous chorioretinal atrophy: Updated scenario;European Journal of Ophthalmology;2023-09-05

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370

www.globalauthorid.com

TOP