@misc{indiciaeabc9dc6f465a,
  title = {PMP22 associates with MPZ via their transmembrane domains and disrupting this interaction causes a loss-of-function phenotype similar to hereditary neuropathy associated with liability to pressure palsies (HNPP).},
  author = {Pashkova, N. and Peterson, T. and Ptak, C. and Winistorfer, S. and Ahern, C. and Shy, M. and Piper, R.},
  year = {2023},
  doi = {10.1101/2023.12.24.573255},
  url = {https://www.biorxiv.org/content/10.1101/2023.12.24.573255v1},
  note = {Source identifier: 10.1101/2023.12.24.573255}
}