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1
AWR101
AWR101
http://dx.doi.org/10.1093/BRAIN/AWR101
Spastic paraplegia in 'dominant optic atrophy plus' phenotype due to OPA1 mutation.
P356
Q53719093-B59A2D38-2E21-4F3F-9E1B-E64BE56869F1
P356
AWR101
http://dx.doi.org/10.1093/BRAIN/AWR101