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Literature summary for 1.3.5.1 extracted from

  • Srirangalingam, U.; Walker, L.; Khoo, B.; Macdonald, F.; Gardner, D.; Wilkin, T.J.; Skelly, R.H.; George, E.; Spooner, D.; Monson, J.P.; Grossman, A.B.; Akker, S.A.; Pollard, P.J.; Plowman, N.; Avril, N.; Berney, D.M.; Burrin, J.M.; Reznek, R.H.; Kumar, V.K.; Maher, E.R.; Chew, S.L.
    Clinical manifestations of familial paraganglioma and phaeochromocytomas in succinate dehydrogenase B gene mutation carriers (2008), Clin. Endocrinol. (Oxf.), 69, 587-596.
    View publication on PubMed

Cloned(Commentary)

Cloned (Comment) Organism
genes SDHD and SDHB, DNA and amino acid sequence determination of healthy individuals and patients with paraganglioma and phaeochromocytomas, several samples, overview Homo sapiens
genes SDHD and SDHB, DNA and amino acid sequence determination of healthy individuals and patients with paraganglioma and phaeochromocytomas, several smaples, overview Homo sapiens

Protein Variants

Protein Variants Comment Organism
additional information clinical manifestations of familial paraganglioma and phaeochromocytomas, that may include papillary renal cell carcinoma and macrovascular disease, in succinate dehydrogenase B gene mutation carriers, SDH-B mutation carriers develop disease early and predominantly in extra-adrenal locations, disease penetrance is incomplete, phenoypes, overview Homo sapiens

Organism

Organism UniProt Comment Textmining
Homo sapiens
-
-
-

Synonyms

Synonyms Comment Organism
SDH
-
Homo sapiens