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...

Descripción completa

Detalles Bibliográficos
Autores principales: Yamaga, Masaya, Takemoto, Minoru, Shoji, Mayumi, Sakamoto, Kenichi, Yamamoto, Masashi, Ishikawa, Takahiro, Koshizaka, Masaya, Maezawa, Yoshiro, Kobayashi, Kazuki, Yokote, Koutaro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5559172/
https://www.ncbi.nlm.nih.gov/pubmed/28738022
http://dx.doi.org/10.18632/aging.101265

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5559172/
https://www.ncbi.nlm.nih.gov/pubmed/28738022
http://dx.doi.org/10.18632/aging.101265

Ejemplares similares