Additional file 2: Table S1. of Analysis of SDHAF3 in familial and sporadic pheochromocytoma and paraganglioma

Summary of SDHAF3 c.157 T > C (p.Phe53Leu) variant analysis in familial SDH-associated individuals. Twenty-three unrelated individuals with SDH germline mutations and evidence of disease (i.e. presence of pheochromocytoma and/or paraganglioma) were assessed (using massively parallel sequencing and/or Sanger sequencing) for the presence of SDHAF3 c.157 T > C. (PDF 236 kb

Additional file 1: Table S2. of Analysis of SDHAF3 in familial and sporadic pheochromocytoma and paraganglioma

Summary of SDHAF3 c.157 T > C (p.Phe53Leu) variant analysis in pheochromocytoma and/or paraganglioma of suspected sporadic origin. Fifteen pheochromoctyomas and/or paragangliomas of apparently sporadic origin were assessed (using massively parallel sequencing and/or Sanger sequencing) for the presence of SDHAF3 c.157 T > C. (PDF 119 kb