Open AccessPrimary Hyperparathyroidism in a Patient With Bilateral Pheochromocytoma and a Mutation in the Tumor Suppressor MAX
Author(s) -
Nipith Charoenngam,
Michael Mannstadt
Publication year - 2022
Publication title -
jcem case reports
Language(s) - English
Resource type - Journals
ISSN - 2755-1520
DOI - 10.1210/jcemcr/luad006
Subject(s) - primary hyperparathyroidism , pheochromocytoma , medicine , germline mutation , frameshift mutation , hyperparathyroidism , endocrinology , mutation , exon , pathology , biology , genetics , gene
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