Author:
Pollard P.J.,Brière J.J.,Alam N.A.,Barwell J.,Barclay E.,Wortham N.C.,Hunt T.,Mitchell M.,Olpin S.,Moat S.J.,Hargreaves I.P.,Heales S.J.,Chung Y.L.,Griffiths J.R.,Dalgleish A.,McGrath J.A.,Gleeson M.J.,Hodgson S.V.,Poulsom R.,Rustin P.,Tomlinson I.P.M.
Publisher
Oxford University Press (OUP)
Subject
Genetics(clinical),Genetics,Molecular Biology,General Medicine
Reference38 articles.
1. Rustin, P. (2002) Mitochondria, from cell death to proliferation. Nat. Genet., 30, 352–353.
2. Baysal, B.E., Ferrell, R.E., Willett-Brozick, J.E., Lawrence, E.C., Myssiorek, D., Bosch, A., van der Mey, A., Taschner, P.E., Rubinstein, W.S., Myers, E.N. et al. (2000) Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma. Science, 287, 848–851.
3. Gimm, O., Armanios, M., Dziema, H., Neumann, H.P. and Eng, C. (2000) Somatic and occult germ-line mutations in SDHD, a mitochondrial complex II gene, in nonfamilial pheochromocytoma. Cancer Res., 60, 6822–6825.
4. Niemann, S. and Muller, U. (2000) Mutations in SDHC cause autosomal dominant paraganglioma, type 3. Nat. Genet., 26, 268–270.
5. Astuti, D., Latif, F., Dallol, A., Dahia, P.L., Douglas, F., George, E., Skoldberg, F., Husebye, E.S., Eng, C. and Maher, E.R. (2001) Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma. Am. J. Hum. Genet., 69, 49–54.
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