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P157 – 2542: Movement disorder, periventricular nodular heterotopia and putaminal hyperintensity due to an ARFGEF2 gene mutation
Yilmaz, S., Tekin, H., Eraslan, C., Serdaroğlu, G., Tekgul, H., Mancini, G.M.S., Gökben, S.Volume:
19
Language:
english
Journal:
European Journal of Paediatric Neurology
DOI:
10.1016/S1090-3798(15)30470-0
Date:
May, 2015
File:
PDF, 92 KB
english, 2015