Discovering a novel genetic variant in 11 family members who had isolated pheochromocytoma linked to von Hippel-Lindau (VHL) syndrome, aligning with the type 2c phenotype

Hussein Alhawaria Department of Internal Medicine, School of Medicine, The University of Jordan, Amman, JordanCorrespondence[email protected]
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Zaina Obeidata Department of Internal Medicine, School of Medicine, The University of Jordan, Amman, JordanView further author information

Lina Wahbeha Department of Internal Medicine, School of Medicine, The University of Jordan, Amman, JordanView further author information

Ayman Mismarb Department of Special Surgery, School of Medicine, The University of Jordan, Amman, JordanView further author information

Nedal Younisb Department of Special Surgery, School of Medicine, The University of Jordan, Amman, JordanView further author information

Hanan Jafara Department of Internal Medicine, School of Medicine, The University of Jordan, Amman, JordanView further author information

Munther Momania Department of Internal Medicine, School of Medicine, The University of Jordan, Amman, JordanView further author information

Nedal Alsabatinb Department of Special Surgery, School of Medicine, The University of Jordan, Amman, JordanView further author information

Abdalla Awidia Department of Internal Medicine, School of Medicine, The University of Jordan, Amman, JordanView further author information

Hussam Alhawaria Department of Internal Medicine, School of Medicine, The University of Jordan, Amman, JordanView further author information

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