ALDH18A1 gene mutations cause dominant spastic paraplegia SPG9: loss of function effect and plausibility of a dominant negative mechanism.

@article{Panza2016ALDH18A1GM,
  title={ALDH18A1 gene mutations cause dominant spastic paraplegia SPG9: loss of function effect and plausibility of a dominant negative mechanism.},
  author={Emanuele Panza and Juan M Escamilla-Honrubia and Clara Marco-Mar{\'i}n and Nadine Gougeard and Giuseppe De Michele and Vincenzo Brescia Morra and Rocco Liguori and Leonardo Salviati and Maria Alice Donati and Roberto Cusano and Tommaso Pippucci and Roberto Ravazzolo and Andrea H. Nemeth and Sarah F. Smithson and Sally L. Davies and Jane A. Hurst and D. Bordo and Vicente Rubio and Marco Seri},
  journal={Brain : a journal of neurology},
  year={2016},
  volume={139 Pt 1},
  pages={e3}
}

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