Skip to main content
Article thumbnail
Location of Repository

A Chinese family with Oguchi’s disease due to compound heterozygosity including a novel deletion in the arrestin gene

By Lingli Huang, Wen Li, Weilin Tang, Xiaohua Zhu, Pingbo Ou-yang and Guangxiu Lu
Topics: Research Article
Publisher: Molecular Vision
OAI identifier:
Provided by: PubMed Central

Suggested articles


  1. (1995). A homozygous 1-base pair deletion in the arrestin gene is a frequent cause of Oguchi disease in Japanese. Nat Genet
  2. (1965). Oguchi's Disease. Arch Ophthalmol

To submit an update or takedown request for this paper, please submit an Update/Correction/Removal Request.