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  1. No Access

    Article

    The parkin gene and its phenotype

    Mutations of the parkin gene on chromosome 6 cause autosomal recessive, early onset parkinsonism. This is the most frequent form of monogenic parkinsonism so far identified. The associated phenotypical spectrum ...

    V. Bonifati, G. De Michele, C. B. Lücking, A. Dürr, E. Fabrizio… in Neurological Sciences (2001)

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    Article

    Ultrastructural localization of parkin in the rat brainstem, thalamus and basal ganglia

    The parkin gene encodes a 52 kd putative E3 ubiquitin-protein ligase involved in an autosomal recessive form of early onset parkinsonism. Parkin ultrastructural localization was studied by immunohistochemistry in...

    A. Mouatt-Prigent, M.-P. Muriel, W.-J. Gu… in Journal of Neural Transmission (2004)

  3. No Access

    Article

    Polymorphisms in the proteasomal subunit alpha4 are not associated with Parkinson's disease

    C. B. Lücking, P. Lichtner, M. Dichgans, T. Illig, C. Gieger… in Journal of Neurology (2008)