First report of OPA1 screening in Greek patients with autosomal dominant optic atrophy and identification of a previously undescribed OPA1 mutation.
Kamakari, Smaragda, Koutsodontis, George, Tsilimbaris, Miltiadis, Fitsios, Athanasios, Chrousos, GeorgiaVolume:
20
Year:
2014
Language:
english
Journal:
Molecular vision
DOI:
10.0000/PMID24883014
File:
PDF, 1.08 MB
english, 2014