International SDH Consortium — During the past three years, mutations have been identified in SDHB and SDHD (genes encoding for SDHB and SDHD, component peptides of mitochondrial complex II) in patients with familial pheochromocytoma and apparently sporadic pheochromocytoma. We have established an International SDH Consortium and are seeking international cooperation and treatment and study of patients with these diseases.

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