An inherited hypomorphic variant in PIEZO2 reveals structural features of mechanotransduction.
By explaining how a single amino acid change produces a hypomorphic PIEZO2 allele, the findings broaden the clinical spectrum of PIEZO2 disorders and offer structural insight into mechanotransduction.
Alec R. Nickolls, Eric M. Mulhall, Daniel J. Orlin et al.
· Neuron · 0 citations