Author:
Srirangalingam Umasuthan,Walker Lisa,Khoo Bernard,MacDonald Fiona,Gardner Daphne,Wilkin Terence J.,Skelly Robert H.,George Emad,Spooner David,Monson John P.,Grossman Ashley B.,Akker Scott A.,Pollard Patrick J.,Plowman Nick,Avril Norbert,Berney Daniel M.,Burrin Jacky M.,Reznek Rodney H.,Kumar V.K. Ajith,Maher Eamonn R.,Chew Shern L.
Subject
Endocrinology, Diabetes and Metabolism,Endocrinology
Reference27 articles.
1. 1DeLellis, R.A., Lloyd,.R.V., Heitz, P.U. & Eng, C. (eds.) (2004) Tumours of Endocrine Organs. Pathology and Genetics. World Health Organization, IARC Press, Lyon.
2. Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma;Baysal;Science,2000
3. Mutations in SDHC cause autosomal dominant paraganglioma, type 3;Niemann;Nature Genetics,2000
4. Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma;Astuti;American Journal of Human Genetics,2001
5. Mitochondria and apoptosis;Green;Science,1998
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