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Updated: Oct 28, 2025

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Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease
Published on: April 4, 2018
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A patient with RET D631Y mutation present with pheochromocytoma
1Department of Internal Medicine Sanggye Paik Hospital Inje University College of Medicine Seoul Korea.
Clinical Case Reports
|July 16, 2021
Abstract:
Patients with MEN2A with RET D631Y mutation most commonly present with pheochromocytomas. MTC is a less common part of the syndrome. Therefore, MEN2A caused by the RET D631Y mutation would be a benign nature.
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