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Phosphodiesterase 2A and 3B variants are associated with primary aldosteronism
Familial primary aldosteronism (PA) is rare and mostly diagnosed in early-onset hypertension (HT). However, “sporadic” bilateral adrenal hyperplasia (BAH) is the most frequent cause of PA and remains without genetic etiology in most cases. Our aim was to investigate new genetic defects associated wi...
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| Izdano u: | Endocr Relat Cancer |
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| Glavni autori: | , , , , , , , , , , , , , , , , , , , , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
2021
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| Teme: | |
| Online pristup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7757641/ https://ncbi.nlm.nih.gov/pubmed/33112806 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1530/ERC-20-0384 |
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