Genetic Diseases of PIEZO1 and PIEZO2 Dysfunction
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Elsevier
Reference121 articles.
1. Plug-N-Play: Mechanotransduction goes modular;Akyuz;Neuron,2016
2. Mutations in NALCN cause an autosomal-recessive syndrome with severe hypotonia, speech impairment, and cognitive delay;Al-Sayed;American Journal of Human Genetics,2013
3. Dehydrated hereditary stomatocytosis linked to gain-of-function mutations in mechanically activated PIEZO1 ion channels;Albuisson;Nature Communications,2013
4. Screening for mutations in PIEZO2 that cause Distal Arthrogryposis Type 5;Almanza,2014
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