Associated Papers
Clinical exome next‑generation sequencing panel for hereditary pheochromocytoma and paraganglioma diagnosis.
Melli B et al.
Experimental and Therapeutic Medicine, 2025
Succinate dehydrogenase variants in paraganglioma: why are B subunit variants 'bad'?
Gruber LM et al.
Endocrine Oncology (bristol, England), 2023
37434649 (PubMed )
Supplement: supplementary_table_1.xlsx › Missense_Variants
Functional analysis of clinical BARD1 germline variants.
Toh MR et al.
Cold Spring Harbor Molecular Case Studies, 2019
31371347 (PubMed )
Supplement: supp_mcs.a004093_Supplemental_Materials.docx
Overview of mitochondrial germline variants and mutations in human disease: Focus on breast cancer (Review).
Jiménez-Morales S et al.
International Journal of Oncology, 2018
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