Phenotypic variability in three families with valosin-containing protein mutation.
Spina, S.; Laar, A. D.; Murrell, J. R.; Hamilton, R. L.; Kofler, J. K.; Epperson, F.; Farlow, M. R.; Lopez, O. L.; Quinlan, J.; DeKosky, S. T.; Ghetti, B.; European Journal of Neurology, 2013, vol. 20, issue 2, p 251, ISSN 13515101. ISBN 14681331.

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