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P89 – 2878: Neuronal ceroid lipofuscinosis-2 (CLN2) natural history and path to diagnosis: International experts' current experience and recommendations on CLN2 disease, a type of Batten disease, resulting from TPP1 enzyme deficiency
Schulz, A., Miller, N., Mole, S.E., Cohen-Pfeffer, J.L.Volume:
19
Language:
english
Journal:
European Journal of Paediatric Neurology
DOI:
10.1016/S1090-3798(15)30402-5
Date:
May, 2015
File:
PDF, 81 KB
english, 2015