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% Source: https://alzhub.org/research?journal=Orphanet+journal+of+rare+diseases
% 3 entries, in the order the page lists them. Built from alzhub.org's own records.
% 0 entries have no readable author in the source record and carry no author field.

@article{hayer2017-28193273,
  author  = {Hayer, S. N. and Deconinck, T. and Bender, B. and Smets, K. and Züchner, S. and Reich, S. and Schöls, L. and Schüle, R. and others},
  title   = {{STUB1/CHIP mutations cause Gordon Holmes syndrome as part of a widespread multisystemic neurodegeneration: evidence from four novel mutations}},
  journal = {Orphanet journal of rare diseases},
  year    = {2017},
  doi     = {10.1186/s13023-017-0580-x},
  pmid    = {28193273},
  url     = {https://doi.org/10.1186/s13023-017-0580-x}
}

@article{roos2010-21171977,
  author  = {Roos, R. A.},
  title   = {{Huntington's disease: a clinical review}},
  journal = {Orphanet journal of rare diseases},
  year    = {2010},
  doi     = {10.1186/1750-1172-5-40},
  pmid    = {21171977},
  url     = {https://doi.org/10.1186/1750-1172-5-40}
}

@article{vanier2010-20525256,
  author  = {Vanier, M. T.},
  title   = {{Niemann-Pick disease type C}},
  journal = {Orphanet journal of rare diseases},
  year    = {2010},
  doi     = {10.1186/1750-1172-5-16},
  pmid    = {20525256},
  url     = {https://doi.org/10.1186/1750-1172-5-16}
}