TY  - RPRT
TI  - 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).
AU  - Pashkova, N.
AU  - Peterson, T.
AU  - Ptak, C.
AU  - Winistorfer, S.
AU  - Ahern, C.
AU  - Shy, M.
AU  - Piper, R.
PY  - 2023
DO  - 10.1101/2023.12.24.573255
UR  - https://www.biorxiv.org/content/10.1101/2023.12.24.573255v1
ID  - 10.1101/2023.12.24.573255
ER  -