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A novel mutation (LEU396ARG) in OPA1 is associated with a severe phenotype in a large dominant optic atrophy pedigree Click to show full abstract
A novel mutation (LEU396ARG) in OPA1 is associated with a severe phenotype in a large dominant optic atrophy pedigree
Keywords:
novel mutation;
severe phenotype;
opa1 associated;
leu396arg opa1;
mutation leu396arg;
associated severe
Journal Title: Eye
Year Published: 2018
Link to full text (if available)
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Journal Title: Eye
Year Published: 2018
Link to full text (if available)
Share on Social Media: Sign Up to like & get
recommendations!