An Alu-mediated partial SDHC deletion causes familial and sporadic paraganglioma

Lignende værker

• Prevalence of SDHB, SDHC, and SDHD germline mutations in clinic patients with head and neck paragangliomas
  af: Baysal, B, et al.
  Udgivet: (2002)
• Mutation analysis of SDHB and SDHC: novel germline mutations in sporadic head and neck paraganglioma and familial paraganglioma and/or pheochromocytoma
  af: Bayley, Jean-Pierre, et al.
  Udgivet: (2006)
• Aberrant Splicing of SDHC in Families With Unexplained Succinate Dehydrogenase-Deficient Paragangliomas
  af: De Sousa, Sunita M C, et al.
  Udgivet: (2020)
• A SDHC Founder Mutation Causes Paragangliomas (PGLs) in the French Canadians: New Insights on the SDHC-Related PGL
  af: Bourdeau, Isabelle, et al.
  Udgivet: (2016)
• Analysis of SDHAF3 in familial and sporadic pheochromocytoma and paraganglioma
  af: Dwight, Trisha, et al.
  Udgivet: (2017)