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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Detalles Bibliográficos
Autores principales: Vitale, Alessandra Maria, Conway de Macario, Everly, Alessandro, Riccardo, Cappello, Francesco, Macario, Alberto J. L., Marino Gammazza, Antonella
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7461820/
https://www.ncbi.nlm.nih.gov/pubmed/33014020
http://dx.doi.org/10.3389/fgene.2020.00969

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7461820/
https://www.ncbi.nlm.nih.gov/pubmed/33014020
http://dx.doi.org/10.3389/fgene.2020.00969

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