Abstract
In vitro studies with purified mutant Hsp60 proteins and in vivo studies with gene-modified mice and patient and model cells have revealed some of the molecular mechaisms underlying Hsp60 deficiency in humans.
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Bross, P. (2015). Molecular Investigations of Disease Mechanisms. In: The Hsp60 Chaperonin. SpringerBriefs in Molecular Science(). Springer, Cham. https://doi.org/10.1007/978-3-319-26088-4_15
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DOI: https://doi.org/10.1007/978-3-319-26088-4_15
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Publisher Name: Springer, Cham
Print ISBN: 978-3-319-26086-0
Online ISBN: 978-3-319-26088-4
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