A Novel CCT5 Missense Variant Associated with Early Onset Motor Neuropathy

A Novel CCT5 Missense Variant Associated with Early Onset Motor Neuropathy

Diseases associated with acquired or genetic defects in members of the chaperoning system (CS) are increasingly found and have been collectively termed chaperonopathies. Illustrative instances of genetic chaperonopathies involve the genes for chaperonins of Groups I (e.g., Heat shock protein 60, <...

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Bibliographic Details
Main Authors: Vincenzo Antona, Federica Scalia, Elisa Giorgio, Francesca C. Radio, Alfredo Brusco, Massimiliano Oliveri, Giovanni Corsello, Fabrizio Lo Celso, Maria Vadalà, Everly Conway de Macario, Alberto J. L. Macario, Francesco Cappello, Mario Giuffrè
Format: Article
Language:English
Published: MDPI AG 2020-10-01
Series:International Journal of Molecular Sciences
Subjects:
CCT5
chaperonins
chaperoning system
genetic variants
mutation
genetic chaperonopathies
Online Access:https://www.mdpi.com/1422-0067/21/20/7631

Internet

https://www.mdpi.com/1422-0067/21/20/7631

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