Skip to main content
Abnormal retinal development associated with FRMD7 mutations.
Published Web Location
http://europepmc.org/articles/PMC4082370?pdf=renderNo data is associated with this publication.
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
Many UC-authored scholarly publications are freely available on this site because of the UC's open access policies. Let us know how this access is important for you.