A novel mutation (LEU396ARG) in OPA1 is associated with a...

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Eye 2018 / 01

A novel mutation (LEU396ARG) in OPA1 is associated with a severe phenotype in a large dominant optic atrophy pedigree

Schnieders, M J, Goar, W, Griess, M, Roos, B R, Scheetz, T E, Stone, E M, Fingert, J H
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Language:
english
Journal:
Eye
DOI:
10.1038/eye.2017.303
Date:
January, 2018
File:
PDF, 344 KB
english, 2018
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