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)
Preprint in bioRxiv (December 2023)
The most recent citing publications are shown below. View all 10 publications that cite this research output on Dimensions.
Preprint in bioRxiv (December 2023)
Article in International Journal of Molecular Sciences (December 2022)
Article in Experimental Hematology & Oncology (October 2022)