Search Results - Schneiders, Marit S

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  1. 1
    Mutational spectrum and genotype-phenotype correlations in mevalonate kinase deficiency

    Mutational spectrum and genotype-phenotype correlations in mevalonate kinase deficiency by Mandey, Saskia H.L., Schneiders, Marit S., Koster, Janet, Waterham, Hans R.

    Published in Human mutation
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  2. 2
    Regulation of Isoprenoid/Cholesterol Biosynthesis in Cells from Mevalonate Kinase-deficient Patients

    Regulation of Isoprenoid/Cholesterol Biosynthesis in Cells from Mevalonate Kinase-deficient Patients by Houten, Sander M, Schneiders, Marit S, Wanders, Ronald J A, Waterham, Hans R

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  3. 3
    Manipulation of isoprenoid biosynthesis as a possible therapeutic option in mevalonate kinase deficiency

    Manipulation of isoprenoid biosynthesis as a possible therapeutic option in mevalonate kinase deficiency by Schneiders, Marit S., Houten, Sander M., Turkenburg, Marjolein, Wanders, Ronald J. A., Waterham, Hans R.

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