Letter to the Editor: “A Unique Case of Metastatic, Functional, Hereditary Paraganglioma Associated With an SDHC Germline Mutation”

Gelijkaardige items

• A Unique Case of Metastatic, Functional, Hereditary Paraganglioma Associated With anSDHC Germline Mutation
  door: Ong, Raquel Kristin S, et al.
  Gepubliceerd in: (2018)
• Mutation analysis of SDHB and SDHC: novel germline mutations in sporadic head and neck paraganglioma and familial paraganglioma and/or pheochromocytoma
  door: Bayley, Jean-Pierre, et al.
  Gepubliceerd in: (2006)
• SAT-315 SDHC Germline Mutation Carrier with Primary Paraganglioma of the Thyroid Gland
  door: Lee, Hyunju, et al.
  Gepubliceerd in: (2019)
• Prevalence of SDHB, SDHC, and SDHD germline mutations in clinic patients with head and neck paragangliomas
  door: Baysal, B, et al.
  Gepubliceerd in: (2002)
• The Clinical Phenotype of SDHC-Associated Hereditary Paraganglioma Syndrome (PGL3)
  door: Else, Tobias, et al.
  Gepubliceerd in: (2014)