Identification of eight novel SDHB, SDHC, SDHD germline variants in Danish pheochromocytoma/paraganglioma patients

Medicin og biovidenskab

• Paraganglioma 100%
• Pheochromocytoma 87%
• Succinate Dehydrogenase 49%
• Exome 47%
• Loss of Heterozygosity 45%
• Germ-Line Mutation 44%
• Missense Mutation 40%
• High-Throughput Nucleotide Sequencing 37%
• Computer Simulation 37%
• Risk Assessment 32%
• Genes 31%
• Population 30%
• Databases 23%
• Mutation 21%