Leber Hereditary Optic Neuropathy Caused by a Mitochondrial DNA 10663T>C Point Mutation and Its Response to Idebenone Treatment
- PMID: 29210930
- DOI: 10.1097/WNO.0000000000000598
Leber Hereditary Optic Neuropathy Caused by a Mitochondrial DNA 10663T>C Point Mutation and Its Response to Idebenone Treatment
Comment in
-
Leber Hereditary Optic Neuropathy in a Mother and Daughter Associated With m.10197G>A Mutation.J Neuroophthalmol. 2019 Mar;39(1):142. doi: 10.1097/WNO.0000000000000714. J Neuroophthalmol. 2019. PMID: 30199507 No abstract available.
Comment on
-
International Consensus Statement on the Clinical and Therapeutic Management of Leber Hereditary Optic Neuropathy.J Neuroophthalmol. 2017 Dec;37(4):371-381. doi: 10.1097/WNO.0000000000000570. J Neuroophthalmol. 2017. PMID: 28991104
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources