A novel H101Q mutation causes PKCγ loss in spinocerebellar ataxia type 14

  • Isabel Alonso, Cristina Costa, André Gomes, Anabela Ferro, Ana I. Seixas, Sérgio Silva, Vitor Tedim Cruz, Paula Coutinho, Jorge Sequeiros, Isabel Silveira
  • Journal of Human Genetics, September 2005, Springer Science + Business Media
  • DOI: 10.1007/s10038-005-0287-z

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The following have contributed to this page: Dr Sérgio Estrela Silva and Jorge Sequeiros

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