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  1. 1
    TSC1 and TSC2 mutations in tuberous sclerosis, the associated phenotypes and a model to explain observed TSC1/TSC2 frequency ratios

    TSC1 and TSC2 mutations in tuberous sclerosis, the associated phenotypes and a model to explain observed TSC1/TSC2 frequency ratios von LANGKAU, Nicola, MARTIN, Nicola, ZIMMERHACKL, Lothar Bernd, JANSSEN, Bart, BRANDT, Regine, ZÜGGE, Karin, QUAST, Stefanie, WIEGELE, Gerd, JAUCH, Anna, REHM, Marion, KUHL, Andrea, MACK-VETTER, Monika

    Veröffentlicht in European journal of pediatrics

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  2. 2
    Molecular genetic investigation of the variability of the GTPase activating protein- (GAP-) related domain of the tuberous sclerosis-2 (TSC2) gene in TSC patients and healthy subjects

    Molecular genetic investigation of the variability of the GTPase activating protein- (GAP-) related domain of the tuberous sclerosis-2 (TSC2) gene in TSC patients and healthy subje...

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