P255 – 1787 Optic atrophy plus, a unique phenotype to a known mutation with early onset and rapid progression
Cohen Rappaport, Y, Blumkin, L, Leshinsky-Silver, E, Lev, D, Lerman-Sagie, TVolume:
17
Language:
english
Journal:
European Journal of Paediatric Neurology
DOI:
10.1016/S1090-3798(13)70434-3
Date:
September, 2013
File:
PDF, 61 KB
english, 2013