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Endocrine Manifestations of Von Hippel–Landau Disease
Von Hippel–Lindau (VHL) disease is an autosomal dominant disorder characterized by various endocrine, nonendocrine, benign, and malignant tumors in various organs. VHL tumor suppressor gene, located on short arm of chromosome 3 is responsible for this. Pheochromocytoma (PCC) is one of the important...
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| Publicat a: | Indian J Endocrinol Metab |
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| Autors principals: | , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Wolters Kluwer - Medknow
2019
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6446673/ https://ncbi.nlm.nih.gov/pubmed/31016171 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/ijem.IJEM_252_18 |
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