Hereditary pheochromocytoma/paraganglioma syndrome with a novel mutation in the succinate dehydrogenase subunit B gene in a Japanese family: two case reports

BACKGROUND: Pheochromocytoma and paraganglioma caused by succinate dehydrogenase gene mutations is called hereditary pheochromocytoma/paraganglioma syndrome. In particular, succinate dehydrogenase subunit B mutations are important because they are strongly associated with the malignant behavior of p...

Descripción completa

Detalles Bibliográficos
Autores principales: Hirose, Rei, Tsurutani, Yuya, Sugisawa, Chiho, Inoue, Kosuke, Suematsu, Sachiko, Nagata, Maki, Hasegawa, Naoki, Kakuta, Yukio, Yonamine, Masato, Takekoshi, Kazuhiro, Kimura, Noriko, Saito, Jun, Nishikawa, Tetsuo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8140422/
https://www.ncbi.nlm.nih.gov/pubmed/34020699
http://dx.doi.org/10.1186/s13256-021-02852-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8140422/
https://www.ncbi.nlm.nih.gov/pubmed/34020699
http://dx.doi.org/10.1186/s13256-021-02852-z

Ejemplares similares