Schnieders, M., Goar, W., Griess, M., Roos, B., Scheetz, T., Stone, E., & Fingert, J. (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)
TE Scheetz
First name:
TE
Last name:
Scheetz