Novel Germline IPHD2/I Variant in a Metastatic Pheochromocytoma and Chronic Myeloid Leukemia, but in...
Novel Germline IPHD2/I Variant in a Metastatic Pheochromocytoma and Chronic Myeloid Leukemia, but in the Absence of Polycythemia
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MDPI AG
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English
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MDPI AG
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Background: Pheochromocytoma (Pheo) and paraganglioma (PGL) are rare tumors, mostly resulting from pathogenic variants of predisposing genes, with a genetic contribution that now stands at around 70%. Germline variants account for approximately 40%, while the remaining 30% is attributable to somatic variants. Objective: This study aimed to describe...
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Novel Germline IPHD2/I Variant in a Metastatic Pheochromocytoma and Chronic Myeloid Leukemia, but in the Absence of Polycythemia
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TN_cdi_gale_infotracmisc_A744897441
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_gale_infotracmisc_A744897441
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ISSN
1648-9144
DOI
10.3390/medicina58081113
