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Using nuclear envelope mutations to explore age-related skeletal muscle weakness
Skeletal muscle weakness is an important determinant of age-related declines in independence and quality of life but its causes remain unclear. Accelerated ageing syndromes such as Hutchinson–Gilford Progerin Syndrome, caused by mutations in genes encoding nuclear envelope proteins, have been extens...
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| Publicado no: | Clin Sci (Lond) |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Portland Press Ltd.
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7450176/ https://ncbi.nlm.nih.gov/pubmed/32844998 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1042/CS20190066 |
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