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% Source: https://alzhub.org/research?author=Andermann+E
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@article{smith2013-23297359,
  author  = {Smith, K. R. and Dahl, H. H. and Canafoglia, L. and Andermann, E. and Damiano, J. and Morbin, M. and Bruni, A. C. and Giaccone, G. and others},
  title   = {{Cathepsin F mutations cause Type B Kufs disease, an adult-onset neuronal ceroid lipofuscinosis}},
  journal = {Human molecular genetics},
  year    = {2013},
  doi     = {10.1093/hmg/dds558},
  pmid    = {23297359},
  url     = {https://doi.org/10.1093/hmg/dds558}
}

@article{cadieuxdion2013-22978711,
  author  = {Cadieux-Dion, M. and Andermann, E. and Lachance-Touchette, P. and Ansorge, O. and Meloche, C. and Barnabé, A. and Kuzniecky, R. I. and Andermann, F. and others},
  title   = {{Recurrent mutations in DNAJC5 cause autosomal dominant Kufs disease}},
  journal = {Clinical genetics},
  year    = {2013},
  doi     = {10.1111/cge.12020},
  pmid    = {22978711},
  url     = {https://doi.org/10.1111/cge.12020}
}