P157 – 2542: Movement disorder, periventricular nodular heterotopia and putaminal hyperintensity due to an ARFGEF2 gene mutation

Conference paper > Summary Text

Authors: S. Yilmaz, H. Tekin, Cenk ERASLAN, G. Serdaroğlu, Hasan TEKGÜL, G.M.S. Mancini, SARENUR GÖKBEN

European Journal of Paediatric Neurology, , , International, Summary Text, WoS, vol 19, pp S138-S138

DOI: 10.1016/s1090-3798(15)30470-0

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