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Article

SDH Subunit Mutation Status in Saliva: Genetic Testing in Patients with Pheochromocytoma.

Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme - 1 Apr 2016

Osinga T E, Xekouki P, Nambuba J, Faucz F R, de la Luz Sierra M, Links T P, Kema I P, Adams K, Stratakis C A, van der Horst-Schrivers A N A, Pacak K

Abstract excerpt

Germline mutations occur in up to 30-40% of pheochromocytoma/paraganglioma, with mutations in the succinate dehydrogenase (SDH) subunits B (SDHB) and D (SDHD) being the most common. Blood samples are favored for obtaining high quality DNA, however, leukocytes can also be obtained by collecting saliva. The aim of this study was to determine whether SDHB and SDHD gene mutations in patients with...

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Source

Identifiers

PMID: 26916530
DOI: 10.1055/s-0035-1569265

Genes

SDHB
SDHD

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

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SDH Subunit Mutation Status in Saliva: Genetic Testing in Patients with Pheochromocytoma.PMID 26916530Read ↗

Mutations of the SDHB and SDHD genes.Semantic proximity Read ↗

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The Succinate Dehydrogenase Genetic Testing in a Large Prospective Series of Patients with ParagangliomasSemantic proximity Read ↗

Succinate Dehydrogenase (SDH)-Deficient Pancreatic Neuroendocrine Tumor Expands the SDH-Related Tumor Spectrum.Semantic proximity Read ↗

International consensus on initial screening and follow-up of asymptomatic SDHx mutation carriersSemantic proximity Read ↗

Simple and rapid characterization of novel large germline deletions in SDHB, SDHC and SDHD-related paraganglioma.Semantic proximity Read ↗

Collection and Extraction of Saliva DNA for Next Generation SequencingSemantic proximity Read ↗

The phenotype of SDHB germline mutation carriers: a nationwide study.Semantic proximity Read ↗

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High Frequency of<i>SDHB</i>Germline Mutations in Patients with Malignant Catecholamine-Producing Paragangliomas: Implications for Genetic TestingSemantic proximity Read ↗

A Novel SDHB IVS2-2A>C Mutation Is Responsible for Hereditary Pheochromocytoma/Paraganglioma Syndrome.Semantic proximity Read ↗

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