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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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1990 | 1 |
1993 | 1 |
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2008 | 1 |
2023 | 1 |
2024 | 0 |
PubMed for id: 256418952
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Hereditary Paraganglioma-Pheochromocytoma Syndromes.
2008 May 21 [updated 2023 Sep 21]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024.
2008 May 21 [updated 2023 Sep 21]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024.
PMID: 20301715
Free Books & Documents.
Review.
Mutations in SDHC cause autosomal dominant paraganglioma, type 3.
Niemann S, Müller U.
Niemann S, et al.
Nat Genet. 2000 Nov;26(3):268-70. doi: 10.1038/81551.
Nat Genet. 2000.
PMID: 11062460
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Characterization of the human SDHC gene encoding of the integral membrane proteins of succinate-quinone oxidoreductase in mitochondria.
Elbehti-Green A, Au HC, Mascarello JT, Ream-Robinson D, Scheffler IE.
Elbehti-Green A, et al.
Gene. 1998 Jun 15;213(1-2):133-40. doi: 10.1016/s0378-1119(98)00186-3.
Gene. 1998.
PMID: 9714607
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Cytochrome b in human complex II (succinate-ubiquinone oxidoreductase): cDNA cloning of the components in liver mitochondria and chromosome assignment of the genes for the large (SDHC) and small (SDHD) subunits to 1q21 and 11q23.
Hirawake H, Taniwaki M, Tamura A, Kojima S, Kita K.
Hirawake H, et al.
Cytogenet Cell Genet. 1997;79(1-2):132-8. doi: 10.1159/000134700.
Cytogenet Cell Genet. 1997.
PMID: 9533030
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Human complex II (succinate-ubiquinone oxidoreductase): cDNA cloning of iron sulfur (Ip) subunit of liver mitochondria.
Kita K, Oya H, Gennis RB, Ackrell BA, Kasahara M.
Kita K, et al.
Biochem Biophys Res Commun. 1990 Jan 15;166(1):101-8. doi: 10.1016/0006-291x(90)91916-g.
Biochem Biophys Res Commun. 1990.
PMID: 2302193
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