A Typical Case Presentation with Spontaneous Visual Recovery in Patient Diagnosed with Leber Hereditary Optic Neuropathy due to Rare Point Mutation in MT-ND4 Gene (m.11253T>C) and Literature Review.
- DOI
- 10.3390/medicina57030202
- Published
- 2021 Feb 26
- Container
- Medicina (Kaunas, Lithuania)
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.3390/medicina57030202,
title = {A Typical Case Presentation with Spontaneous Visual Recovery in Patient Diagnosed with Leber Hereditary Optic Neuropathy due to Rare Point Mutation in MT-ND4 Gene (m.11253T>C) and Literature Review.},
author = {Liutkeviciene R and Sidaraite A and Kuliaviene L and Glebauskiene B and Jurkute N and Aluzaite-Baranauskiene L and Gelzinis A and Zemaitiene R},
year = {2021},
journal = {Medicina (Kaunas, Lithuania)},
doi = {10.3390/medicina57030202},
url = {https://doi.org/10.3390/medicina57030202}
}RIS
TY - JOUR TI - A Typical Case Presentation with Spontaneous Visual Recovery in Patient Diagnosed with Leber Hereditary Optic Neuropathy due to Rare Point Mutation in MT-ND4 Gene (m.11253T>C) and Literature Review. AU - Liutkeviciene R AU - Sidaraite A AU - Kuliaviene L AU - Glebauskiene B AU - Jurkute N AU - Aluzaite-Baranauskiene L AU - Gelzinis A AU - Zemaitiene R PY - 2021 JO - Medicina (Kaunas, Lithuania) DO - 10.3390/medicina57030202 UR - https://doi.org/10.3390/medicina57030202 ER -
APA
R, L., A, S., L, K., B, G., N, J., L, A., A, G., & R, Z. (2021). A Typical Case Presentation with Spontaneous Visual Recovery in Patient Diagnosed with Leber Hereditary Optic Neuropathy due to Rare Point Mutation in MT-ND4 Gene (m.11253T>C) and Literature Review.. Medicina (Kaunas, Lithuania). https://doi.org/10.3390/medicina57030202
Source records
- pubmed · retrieved 2026-09-27T07:04:29.990Z