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Next-generation sequencing for the diagnosis of hereditary pheochromocytoma and paraganglioma syndromes
PURPOSE OF REVIEW: About 40% of the neuroendocrine tumors pheochromocytomas and paragangliomas (PPGLs) are caused by an inherited mutation. Diagnostic genetic screening is recommended for patients and their families. However, the number of susceptibility genes involved is high and continues to grow,...
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| 出版年: | Curr Opin Endocrinol Diabetes Obes |
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| 主要な著者: | , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
2015
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7216557/ https://ncbi.nlm.nih.gov/pubmed/25871962 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MED.0000000000000150 |
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