A novel mutation (LEU396ARG) in OPA1 is associated with a severe phenotype in a large dominant optic atrophy pedigree
Crossref DOI link: https://doi.org/10.1038/eye.2017.303
Published Online: 2018-01-19
Published Print: 2018-04
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Schnieders, M J
Goar, W
Griess, M
Roos, B R
Scheetz, T E
Stone, E M
Fingert, J H
Text and Data Mining valid from 2018-01-19
Article History
First Online: 19 January 2018
Competing interests
: The authors declare no conflict of interest.