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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Detalhes bibliográficos
Publicado no:Aging (Albany NY)
Main Authors: Yamaga, Masaya, Takemoto, Minoru, Shoji, Mayumi, Sakamoto, Kenichi, Yamamoto, Masashi, Ishikawa, Takahiro, Koshizaka, Masaya, Maezawa, Yoshiro, Kobayashi, Kazuki, Yokote, Koutaro
Formato: Artigo
Idioma:Inglês
Publicado em: Impact Journals LLC 2017
Assuntos:
Research Paper
Acesso em linha: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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