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

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Journal

Blood Pressure

Topics

Biology

Bioinformatics

Medicine

Cancer Oncology

Internal Medicine

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DOI

10.1080/08037051.2024.2355268

License

CC-BY-NC

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