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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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| Gepubliceerd in: | Front Genet |
|---|---|
| Hoofdauteurs: | , , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Frontiers Media S.A.
2020
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| Onderwerpen: | |
| Online toegang: | 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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