Functional consequences of a SDHB gene mutation in an apparently sporadic pheochromocytoma. [electronic resource]
- The Journal of clinical endocrinology and metabolism Oct 2002
- 4771-4 p. digital
Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
0021-972X
10.1210/jc.2002-020525 doi
Adrenal Gland Neoplasms--enzymology Basic Helix-Loop-Helix Transcription Factors Chromosomes, Human, Pair 1 DNA Mutational Analysis Electron Transport Complex II Endothelial Growth Factors--genetics Female Gene Expression Germ-Line Mutation Humans Immunohistochemistry In Situ Hybridization Iron-Sulfur Proteins--genetics Loss of Heterozygosity Lymphokines--genetics Middle Aged Multienzyme Complexes--deficiency Mutation Mutation, Missense Oxidoreductases--deficiency Pheochromocytoma--enzymology Protein Subunits RNA, Messenger--analysis Sequence Analysis, DNA Succinate Dehydrogenase--deficiency Tomography, X-Ray Computed Trans-Activators--genetics Vascular Endothelial Growth Factor A Vascular Endothelial Growth Factors