Article info

Original research
International initiative for a curated SDHB variant database improving the diagnosis of hereditary paraganglioma and pheochromocytoma

Authors

  1. Correspondence to Dr Nelly Burnichon, Team 13, UMR970 PARCC-HEGP, 75015 Paris, France; nelly.burnichon{at}inserm.fr
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Citation

Ben Aim L, Maher ER, Cascon A, et al
International initiative for a curated SDHB variant database improving the diagnosis of hereditary paraganglioma and pheochromocytoma

Publication history

  • Received December 16, 2020
  • Accepted July 18, 2021
  • First published August 27, 2021.

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