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Journal Scan / Case Study · October 10, 2019

Concurrent Heterozygous VHL and Transmembrane-Protein-127 Gene Mutation Causes an EPO-Secreting Pheochromocytoma in a Normotensive Patient With Severe Erythrocytosis

Journal of Hypertension

 

Additional Info

Disclosure statements are available on the authors' profiles:

Journal of Hypertension
Concurrent Heterozygous Von-Hippel-Lindau and Transmembrane-Protein-127 Gene Mutation Causing an Erythropoietin-Secreting Pheochromocytoma in a Normotensive Patient With Severe Erythrocytosis
J. Hypertens. 2019 Sep 19;[EPub Ahead of Print], A Negro, G Graiani, D Nicoli, E Farnetti, B Casali, I Verzicco, S Tedeschi, A Ghirarduzzi, V Cannone, LDE Marco, A Filice, G Gemelli, A Giunta, A Cabassi

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

Further Reading