The SDH mutation database: an online resource for succinate dehydrogenase sequence variants involved in pheochromocytoma, paraganglioma and mitochondrial complex II deficiency
<p>Abstract</p> <p>Background</p> <p>The SDHA, SDHB, SDHC and SDHD genes encode the subunits of succinate dehydrogenase (succinate: ubiquinone oxidoreductase), a component of both the Krebs cycle and the mitochondrial respiratory chain. SDHA, a flavoprotein and SDHB, an...
Main Authors: | Devilee Peter, Bayley Jean-Pierre, Taschner Peter EM |
---|---|
Format: | Article |
Language: | English |
Published: |
BMC
2005-11-01
|
Series: | BMC Medical Genetics |
Online Access: | http://www.biomedcentral.com/1471-2350/6/39 |
Similar Items
-
Succinate dehydrogenase‐deficient malignant paraganglioma complicated by succinate dehydrogenase‐deficient renal cell carcinoma
by: Yoshitomo Yamaguchi, et al.
Published: (2022-11-01) -
Clinical manifestations of familial paraganglioma and phaeochromocytomas in succinate dehydrogenase B (SDH-B) gene mutation carriers.
by: Srirangalingam, U, et al.
Published: (2008) -
Hypothesis: Why Different Types of SDH Gene Variants Cause Divergent Tumor Phenotypes
by: Jean-Pierre Bayley, et al.
Published: (2022-06-01) -
Mutation analysis of SDHB and SDHC: novel germline mutations in sporadic head and neck paraganglioma and familial paraganglioma and/or pheochromocytoma
by: Wong Nora, et al.
Published: (2006-01-01) -
Metabolome Profiling by HRMAS NMR Spectroscopy of Pheochromocytomas and Paragangliomas Detects SDH Deficiency: Clinical and Pathophysiological Implications
by: Alessio Imperiale, et al.
Published: (2015-01-01)