Search Results - Rabelink, Gwenda M.

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  1. 1
    Novel PRKCG/SCA14 mutation in a Dutch spinocerebellar ataxia family: Expanding the phenotype

    Novel PRKCG/SCA14 mutation in a Dutch spinocerebellar ataxia family: Expanding the phenotype by Vlak, Monique H.M., Sinke, Richard J., Rabelink, Gwenda M., Kremer, Berry P.H., van de Warrenburg, Bart P.C.

    Published in Movement disorders
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  2. 2
    Eighteen-year follow-up of a patient with partial hypoxanthine phosphoribosyltransferase deficiency and a new mutation

    Eighteen-year follow-up of a patient with partial hypoxanthine phosphoribosyltransferase deficiency and a new mutation by Gregoric, Alojz, Rabelink, Gwenda M, Kokalj Vokac, Nadja, Varda, Natasa Marcun, Zagradisnik, Boris

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