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Functional and pharmacological characterization of human Na(+)-carnitine cotransporter hOCTN2 von Wagner, C A, Lükewille, U, Kaltenbach, S, Moschen, I, Bröer, A, Risler, T, Bröer, S, Lang, F

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17α-Hydroxylase/17,20-Lyase Deficiency Caused by a Novel Homozygous Mutation (Y27Stop) in the Cytochrome CYP17 Gene von Müssig, Karsten, Kaltenbach, Simone, Machicao, Fausto, Maser-Gluth, Christiane, Hartmann, Michaela F., Wudy, Stefan A., Schnauder, Günter, Häring, Hans-Ulrich, Seif, Fritz J., Gallwitz, Baptist

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17alpha-hydroxylase/17,20-lyase deficiency caused by a novel homozygous mutation (Y27Stop) in the cytochrome CYP17 gene von Müssig, Karsten, Kaltenbach, Simone, Machicao, Fausto, Maser-Gluth, Christiane, Hartmann, Michaela F, Wudy, Stefan A, Schnauder, Günter, Häring, Hans-Ulrich, Seif, Fritz J, Gallwitz, Baptist

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17a-hydroxylase/17,20-lyase deficiency caused by a novel homozygous mutation (Y27stop) in the cytochrome CYP17 gene von MÜSSIG, Karsten, KALTENBACH, Simone, MACHICAO, Fausto, MASER-GLUTH, Christiane, HARTMANN, Michaela F, WUDY, Stefan A, SCHNAUDER, Günter, HÄRING, Hans-Ulrich, SEIF, Fritz J, GALLWITZ, Baptist

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Functional and pharmacological characterization of human Na+-carnitine cotransporter hOCTN2 von WAGNER, Carsten A, LUKEWILLE, Ulrike, KALTENBACH, Simone, MOSCHEN, Ivano, BRÖER, Angelika, RISLER, Teut, BRÖER, Stefan, LANG, Florian

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Untersuchungen zur Pathophysiologie der Cystinurie Typ I :Charakterisierung der hrBAT-Mutationen R365W und F648S

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