A Unique Case of Metastatic, Functional, Hereditary Paraganglioma Associated With anSDHC Germline Mutation

समान संसाधन

• Letter to the Editor: “A Unique Case of Metastatic, Functional, Hereditary Paraganglioma Associated With an SDHC Germline Mutation”
  द्वारा: Hannah-Shmouni, Fady, और अन्य
  प्रकाशित: (2018)
• The Clinical Phenotype of SDHC-Associated Hereditary Paraganglioma Syndrome (PGL3)
  द्वारा: Else, Tobias, और अन्य
  प्रकाशित: (2014)
• SAT-315 SDHC Germline Mutation Carrier with Primary Paraganglioma of the Thyroid Gland
  द्वारा: Lee, Hyunju, और अन्य
  प्रकाशित: (2019)
• Next-generation sequencing for the diagnosis of hereditary pheochromocytoma and paraganglioma syndromes
  द्वारा: Toledo, Rodrigo A., और अन्य
  प्रकाशित: (2015)
• Mutation analysis of SDHB and SDHC: novel germline mutations in sporadic head and neck paraganglioma and familial paraganglioma and/or pheochromocytoma
  द्वारा: Bayley, Jean-Pierre, और अन्य
  प्रकाशित: (2006)