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Coexistence of VHL Disease and CPT2 Deficiency: A Case Report

von Hippel-Lindau (VHL) disease is an inherited syndrome manifesting with benign and malignant tumors. Deficiency of carnitine palmitoyltransferase type II (CPT2) is a disorder of lipid metabolism that, in the muscle form, manifests with recurrent attacks of myalgias often associated with myoglobinu...

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Detalles Bibliográficos
Autores principales:	Ferrara, Alfonso Massimiliano, Sciacco, Monica, Zovato, Stefania, Rizzati, Silvia, Colombo, Irene, Boaretto, Francesca, Moggio, Maurizio, Opocher, Giuseppe
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Korean Cancer Association 2016
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5080814/ https://www.ncbi.nlm.nih.gov/pubmed/27034144 http://dx.doi.org/10.4143/crt.2015.450

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