Mutations in LCA5 are an uncommon cause of Leber congenital amaurosis (LCA) type II-Reference-Cited by-同舟云学术

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Mutations in LCA5 are an uncommon cause of Leber congenital amaurosis (LCA) type II

Published:2007 Issue:12 Volume:28 Page:1245-1245
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Gerber Sylvie,Hanein Sylvain,Perrault Isabelle,Delphin Nathalie,Aboussair Nisrine,Leowski Corinne,Dufier Jean-Louis,Roche Olivier,Munnich Arnold,Kaplan Josseline,Rozet Jean-Michel

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/humu.9513/fullpdf

Cited by 20 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. Gene Therapy in Inherited Retinal Diseases: An Update on Current State of the Art;Frontiers in Medicine;2021-10-15

2. Treatment Potential for LCA5-Associated Leber Congenital Amaurosis;Investigative Opthalmology & Visual Science;2020-05-19

3. Knocking out lca5 in zebrafish causes cone-rod dystrophy due to impaired outer segment protein trafficking;Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease;2019-10

4. Amelioration of Neurosensory Structure and Function in Animal and Cellular Models of a Congenital Blindness;Molecular Therapy;2018-06

5. LCA5;Retinal Dystrophy Gene Atlas;2018

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