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: oai:pubmedcentral.nih.gov:3298420
Provided by: PubMed Central
Download PDF:
Sorry, we are unable to provide the full text but you may find it at the following location(s):
  • http://www.pubmedcentral.nih.g... (external link)
  • Suggested articles

    Preview

    Citations

    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.