A novel mutation (LEU396ARG) in OPA1 is associated with a severe phenotype in a large dominant optic atrophy pedigree.
| Author | |
|---|---|
| Year of Publication |
:
2018
|
| Journal |
:
Eye (London, England)
|
| Date Published |
:
2018
|
| ISSN Number |
:
0950-222X
|
| URL |
:
http://dx.doi.org/10.1038/eye.2017.303
|
| DOI |
:
10.1038/eye.2017.303
|
| Short Title |
:
Eye (Lond)
|
| Download citation |
