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Germline SDHB and SDHD mutations in pheochromocytoma and paraganglioma patients
Pheochromocytoma and paragangliomas (PCC/PGL) are neuroendocrine tumors that arise from chromaffin cells of the adrenal medulla and sympathetic/parasympathetic ganglia, respectively. Of clinical relevance regarding diagnosis is the highly variable presentation of symptoms in PCC/PGL patients. To dat...
Gorde:
| Argitaratua izan da: | Endocr Connect |
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| Egile Nagusiak: | , , , , , , , , , , , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
Bioscientifica Ltd
2018
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6240141/ https://ncbi.nlm.nih.gov/pubmed/30352407 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1530/EC-18-0325 |
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