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Items: 15

1.

An Alu-mediated partial SDHC deletion causes familial and sporadic paraganglioma.

Baysal BE, Willett-Brozick JE, Filho PA, Lawrence EC, Myers EN, Ferrell RE.

J Med Genet. 2004 Sep;41(9):703-9. No abstract available. Erratum in: J Med Genet. 2005 Jul;42(7):582.

2.

Autosomal dominant malignant and catecholamine-producing paraganglioma caused by a splice donor site mutation in SDHC.

Niemann S, Müller U, Engelhardt D, Lohse P.

Hum Genet. 2003 Jul;113(1):92-4. Epub 2003 Mar 25.

PMID:
12658451
3.

Assignment of PGL3 to chromosome 1 (q21-q23) in a family with autosomal dominant non-chromaffin paraganglioma.

Niemann S, Becker-Follmann J, Nürnberg G, Rüschendorf F, Sieweke N, Hügens-Penzel M, Traupe H, Wienker TF, Reis A, Müller U.

Am J Med Genet. 2001 Jan 1;98(1):32-6.

PMID:
11426453
4.

Mutations in SDHC cause autosomal dominant paraganglioma, type 3.

Niemann S, Müller U.

Nat Genet. 2000 Nov;26(3):268-70.

PMID:
11062460
5.

PGL3, a third, not maternally imprinted locus in autosomal dominant paraganglioma.

Niemann S, Steinberger D, Müller U.

Neurogenetics. 1999 Sep;2(3):167-70.

PMID:
10541590
6.

A mutation in succinate dehydrogenase cytochrome b causes oxidative stress and ageing in nematodes.

Ishii N, Fujii M, Hartman PS, Tsuda M, Yasuda K, Senoo-Matsuda N, Yanase S, Ayusawa D, Suzuki K.

Nature. 1998 Aug 13;394(6694):694-7.

PMID:
9716135
7.

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.

Gene. 1998 Jun 15;213(1-2):133-40.

PMID:
9714607
9.

Deficiency of complex II of the mitochondrial respiratory chain in late-onset optic atrophy and ataxia.

Taylor RW, Birch-Machin MA, Schaefer J, Taylor L, Shakir R, Ackrell BA, Cochran B, Bindoff LA, Jackson MJ, Griffiths P, Turnbull DM.

Ann Neurol. 1996 Feb;39(2):224-32.

PMID:
8967754
10.

The cDNA sequence of beef heart CII-3, a membrane-intrinsic subunit of succinate-ubiquinone oxidoreductase.

Cochran B, Capaldi RA, Ackrell BA.

Biochim Biophys Acta. 1994 Nov 1;1188(1-2):162-6.

PMID:
7947903
11.
12.

Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency.

Bourgeron T, Rustin P, Chretien D, Birch-Machin M, Bourgeois M, Viegas-Péquignot E, Munnich A, Rötig A.

Nat Genet. 1995 Oct;11(2):144-9.

PMID:
7550341
13.

Assignment of a gene for succinate dehydrogenase to human chromosome 1 by somatic cell hybridization.

Mascarello JT, Soderberg K, Scheffler IE.

Cytogenet Cell Genet. 1980;28(1-2):121-35.

PMID:
6934864
14.

Mitochondrial encephalomyopathy with decreased succinate-cytochrome c reductase activity.

Riggs JE, Schochet SS Jr, Fakadej AV, Papadimitriou A, DiMauro S, Crosby TW, Gutmann L, Moxley RT.

Neurology. 1984 Jan;34(1):48-53.

PMID:
6318158
15.

Defect in succinate oxidation by isolated muscle mitochondria in a patient with symmetrical lesions in the basal ganglia.

Martin JJ, Van de Vyver FL, Scholte HR, Roodhooft AM, Ceuterick C, Martin L, Luyt-Houwen IE.

J Neurol Sci. 1988 Apr;84(2-3):189-200.

PMID:
3379446

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