- Coexistence of VHL Disease and CPT2 Deficiency: A Case Report
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Ferrara AM, Sciacco M, Zovato S, Rizzati S, Colombo I, Boaretto F, Moggio M, Opocher G
- KMID: 2356246
- Cancer Res Treat.
- 2016 Oct;48(4):1438-1442.
- doi: 10.4143/crt.2015.450
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... -
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