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New morphologic and genetic findings in cap disease associated with -tropomyosin (TPM2) mutations
Ohlsson, M., Quijano-Roy, S., Darin, N., Brochier, G., Lacene, E., Avila-Smirnow, D., Fardeau, M., Oldfors, A., Tajsharghi, H.Volume:
71
Language:
english
Journal:
Neurology
DOI:
10.1212/01.wnl.0000336654.44814.b8
Date:
December, 2008
File:
PDF, 832 KB
english, 2008