Missense Mutations of Human Hsp60: A Computational Analysis to Unveil Their Pathological Significance.
Hsp60 gene variants
Hsp60 genetic chaperonopathies
chaperoning system
human genomes
underdiagnosed chaperonopathies
Journal
Frontiers in genetics
ISSN: 1664-8021
Titre abrégé: Front Genet
Pays: Switzerland
ID NLM: 101560621
Informations de publication
Date de publication:
2020
2020
Historique:
received:
07
05
2020
accepted:
31
07
2020
entrez:
5
10
2020
pubmed:
6
10
2020
medline:
6
10
2020
Statut:
epublish
Résumé
Two chaperonopathies have been linked to mutations in the human
Identifiants
pubmed: 33014020
doi: 10.3389/fgene.2020.00969
pmc: PMC7461820
doi:
Types de publication
Journal Article
Langues
eng
Pagination
969Informations de copyright
Copyright © 2020 Vitale, Conway de Macario, Alessandro, Cappello, Macario and Marino Gammazza.
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