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) https://t.co/jOpliB1bl0 https://t.co/eLKA…
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). https://t.co/jabj3yhNaL
"PMP22 and MPZ are like puzzle pieces clicking together in our body. If they don't fit quite right, it can make us feel weak or numb, especially when we bump or squeeze certain body parts. It's like a family trait some people have, called HNPP."
bioArXiv_ 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). https://t.co/nNhlgXaLBa