Article thumbnail

Reply: Spastic paraplegia in ‘dominant optic atrophy plus’ phenotype due to OPA1 mutation

By Patrick Yu-Wai-Man and Patrick F. Chinnery
Topics: Letters to the Editor
Publisher: Oxford University Press
OAI identifier: oai:pubmedcentral.nih.gov:3212709
Provided by: PubMed Central

Suggested articles

Citations

  1. (2010). Multi-system neurological disease is common in patients with OPA1 mutations.
  2. (2011). Pattern of retinal ganglion cell loss in dominant optic atrophy due to OPA1 mutations. Eye 2011. Advance Access published on
  3. (2011). Recent progress in understanding congenital cranial dysinnervation disorders.
  4. (2011). Spastic paraplegia in “dominant optic atrophy plus” phenotype due to OPA1 mutation. Brain

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