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Unraveling the mechanism by which TRPV4 mutations cause skeletal dysplasias

Transient Receptor Potential Vanilloid 4 (TRPV4) is a mechano- and osmosensitive cation channel that is highly expressed in chondrocytes, the cells in cartilage. A large number of mutations in TRPV4 have been linked to skeletal dysplasias, and the goal of this addendum is to shed light on the mechan...

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Detalles Bibliográficos
Autores principales:	Leddy, Holly A, McNulty, Amy L, Guilak, Farshid, Liedtke, Wolfgang
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Taylor & Francis 2014
Materias:	Addendum
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4755236/ https://www.ncbi.nlm.nih.gov/pubmed/26942100 http://dx.doi.org/10.4161/2167549X.2014.962971

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