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Werner syndrome: a model for sarcopenia due to accelerated aging
Werner syndrome (WS) is a rare inheritable progeroid syndrome caused by a mutation in the WRN gene. Although WS has been described as a characteristic appearance of very slender extremities with a stocky trunk, few studies have investigated the loss of muscle mass, fat mass distribution (body compos...
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| Gepubliceerd in: | Aging (Albany NY) |
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| Hoofdauteurs: | , , , , , , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Impact Journals LLC
2017
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5559172/ https://ncbi.nlm.nih.gov/pubmed/28738022 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.18632/aging.101265 |
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