Missense Mutations of Human Hsp60: A Computational Analysis to Unveil Their Pathological Significance

Two chaperonopathies have been linked to mutations in the human hsp60 (hHsp60; HSPD1) gene, but other existing variants might cause diseases, even if there is no comprehensive information about this possibility. To fill this vacuum, which might be at the basis of misdiagnoses or simply ignorance of...

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Detalhes bibliográficos
Publicado no:Front Genet
Main Authors: Vitale, Alessandra Maria, Conway de Macario, Everly, Alessandro, Riccardo, Cappello, Francesco, Macario, Alberto J. L., Marino Gammazza, Antonella
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2020
Assuntos:
Genetics
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7461820/
https://ncbi.nlm.nih.gov/pubmed/33014020
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2020.00969
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