Schnieders, M. J., Goar, W., Griess, M., Roos, B. R., Scheetz, T. E., Stone, E. M., & Fingert, J. H. (2018). A novel mutation (LEU396ARG) in OPA1 is associated with a severe phenotype in a large dominant optic atrophy pedigree. Eye (London, England). https://doi.org/10.1038/eye.2017.303(Original work published 2018)
Klionsky, D. J., Abdelmohsen, K., Abe, A., Abedin, M. J., Abeliovich, H., Arozena, A., et al. Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition). Autophagy, 12(1), 1-222. https://doi.org/10.1080/15548627.2015.1100356(Original work published 2016)
