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Abnormal retinal development associated with FRMD7 mutations.

  • Author(s): Moore, Anthony
  • Thomas, MG
  • Crosier, M
  • Lindsay, S
  • Kumar, A
  • Araki, M
  • Leroy, BP
  • McLean, RJ
  • Sheth, V
  • Maconachie, G
  • Thomas, S
  • et al.

Published Web Location

http://europepmc.org/articles/PMC4082370?pdf=render
No 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

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