Natural and pathogenic protein sequence variation affecting prion-like domains within and across human proteomes
Abstract Background Impaired proteostatic regulation of proteins with prion-like domains (PrLDs) is associated with a variety of human diseases including neurodegenerative disorders, myopathies, and certain forms of cancer. For many of these disorders, current models suggest a prion-like molecular m...
Main Authors: | , |
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Format: | Article |
Language: | English |
Published: |
BMC
2020-01-01
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Series: | BMC Genomics |
Subjects: | |
Online Access: | https://doi.org/10.1186/s12864-019-6425-3 |