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Browsing by Author Smit, L.M.E.

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Full TextIssue DateTitleAuthor(s)
1996Deficiency of the voltage-dependent anion channel: A novel cause of mitochondriopathyHuizing, M.; Ruitenbeek, W.; Thinnes, F.P.; DePinto, V.; Wendel, U., et al
1996A (G-to-A) mutation in the initiation codon of the proteolipid protein gene causing a relatively mild form of Pelizaeus-Merzbacher disease in a Dutch familySistermans, E.A.; Wijs, I.J. de; Coo, R.F.M. de; Smit, L.M.E.; Menko, F.H., et al
1995Spongy white matter changes, MR appearances, differential diagnosis and description of a new diseaseKnaap, M.S. van der; Valk, J.; Barth, P.G.; Smit, L.M.E.; Engelen, B.G.M. van, et al
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