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Article

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

The Tohoku journal of experimental medicine - 1 Jun 2018

Yamanaka Mie, Shiga Kiyoto, Fujiwara Sho, Mizuguchi Yasuhiko, Yasuda Sari, Ishizawa Kota, Saiki Yuriko, Higashi Kenjiro, Ogawa Takenori, Kimura Noriko, Horii Akira

Abstract excerpt

Pheochromocytomas and paragangliomas are neuroendocrine tumors which arise from adrenal medulla, and sympathetic or parasympathetic nerves, respectively. Hereditary cases afflicted by both or either pheochromocytomas and paragangliomas have been reported: these are called hereditary pheochromocytoma/paraganglioma syndromes (HPPS). Many cases of HPPS are caused by mutations of one of the succinate dehydrogenase...

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Source

Identifiers

PMID: 29925701
DOI: 10.1620/tjem.245.99

Genes

SDHB
SDHD

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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