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Role for Germline Mutations and a Rare Coding Single Nucleotide Polymorphism Within KCNJ5 Potassium Channel in a Large Cohort of Sporadic Cases of Primary Aldosteronism.
✍ Scribed by Gianmichele, G.; O’Shaughenessy, K.; Murthy, M.
- Book ID
- 126773145
- Publisher
- Elsevier Science
- Year
- 2014
- Tongue
- English
- Weight
- 87 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0149-2918
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