학술논문
Abnormal retinal development associated with FRMD7 mutations.
Document Type
article
Author
Source
Subject
Language
Abstract
Idiopathic infantile nystagmus (IIN) is a genetically heterogeneous disorder, often associated with FRMD7 mutations. As the appearance of the retina is reported to be normal based on conventional fundus photography, IIN is postulated to arise from abnormal