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Pheochromocytoma in Congenital Cyanotic Heart Disease
Studies on genome-wide transcription patterns have shown that many genetic alterations implicated in pheochromocytoma-paraganglioma (P-PGL) syndromes cluster in a common cellular pathway leading to aberrant activation of molecular response to hypoxia in normoxic conditions (the pseudohypoxia hypothe...
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| Publicado no: | Case Rep Endocrinol |
|---|---|
| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Hindawi
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6176301/ https://ncbi.nlm.nih.gov/pubmed/30356369 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2018/2091257 |
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