Clinical Presentations, Biochemical Phenotypes, and Genotype-Phenotype Correlations in Patients withSuccinate Dehydrogenase Subunit B-Associated Pheochromocytomas and Paragangliomas

Author:

Timmers Henri J. L. M.12,Kozupa Anna1,Eisenhofer Graeme3,Raygada Margarita4,Adams Karen T.1,Solis Daniel1,Lenders Jacques W. M.5,Pacak Karel1

Affiliation:

1. Reproductive Biology and Medicine Branch (H.J.L.M.T., A.K., K.T.A., D.S., K.P.), National Institutes of Health, Bethesda, Maryland 20892-1109

2. Division of General Internal Medicine, and Department of Endocrinology (H.J.L.M.T.), Radboud University Nijmegen Medical Centre, 6500 HB Nijmegen, The Netherlands

3. National Institute of Child Health and Human Development, Clinical Neurocardiology Section (G.E.), National Institutes of Health, Bethesda, Maryland 20892-1109

4. National Institute of Neurological Disorders and Stroke, and Laboratory of Clinical Genetics (M.R.), National Institutes of Health, Bethesda, Maryland 20892-1109

5. Department of Internal Medicine (J.W.M.L.), Radboud University Nijmegen Medical Centre, 6500 HB Nijmegen, The Netherlands

Publisher

The Endocrine Society

Subject

Biochemistry, medical,Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference39 articles.

1. Pheochromocytoma;Pacak;In: Textbook of endocrinology. 5th ed. Philadelphia: Elsevier Saunders, Inc.;,2005

2. Phaeochromocytoma.;Lenders;Lancet,2005

3. Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma.;Baysal;Science,2000

4. Gene mutations in the succinate dehydrogenase subunit SDHB cause susceptibility to familial pheochromocytoma and to familial paraganglioma.;Astuti;Am J Hum Genet,2001

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