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Pontocerebellar hypoplasia type 1: Clinical spectrum and relevance of EXOSC3 mutations
Rudnik-Schoneborn, S., Senderek, J., Jen, J. C., Houge, G., Seeman, P., Puchmajerova, A., Graul-Neumann, L., Seidel, U., Korinthenberg, R., Kirschner, J., Seeger, J., Ryan, M. M., Muntoni, F., SteinliVolume:
80
Language:
english
Journal:
Neurology
DOI:
10.1212/wnl.0b013e31827f0f66
Date:
January, 2013
File:
PDF, 632 KB
english, 2013