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Ravi Das, Shatabdi Bhattacharjee, Jamin M. Letcher, Jenna M. Harris, Sumit Nanda, Istvan Foldi, Erin N. Lottes, Hansley M. Bobo, Benjamin D. Grantier, József Mihály, Giorgio A. Ascoli, Daniel N. Cox
Development (2021) 148 (16): dev187609.
Published: 13 August 2021
... in the localization of dendritic mitochondria, satellite Golgi, and the TRPA channel Painless. Form3 directly interacts with MTs via FH1-FH2 domains. Mutations in human inverted formin 2 ( INF2 ; ortholog of form3 ) have been causally linked to Charcot–Marie–Tooth (CMT) disease. CMT sensory neuropathies lead...
Includes: Supplementary data