| 1 | FHA3, KCNJ5
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| A novel Y152C KCNJ5 mutation responsible for familial hyperaldosteronism type III.
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| Monticone S, Hattangady NG, Penton D, Isales C, Edwards MA, Williams TA, Sterner C, Warth R, Mulatero P, Rainey WE.
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| J Clin Endocrinol Metab Clin Endocrinol Metab. 2013 Sep 13. [Epub ahead of print]
2013
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| 2 | FHA3, KCNJ5
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| Role of KCNJ5 in familial and sporadic primary aldosteronism.
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| Mulatero P, Monticone S, Rainey WE, Veglio F, Williams TA.
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| Nat Rev Endocrinol 9(2):104-12. doi: 10.1038/nrendo.2012.230. Epub 2012 Dec 11. Review.
2013
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| 3 | FHA3, KCNJ5
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| Hypertension with or without adrenal hyperplasia due to different inherited mutations in the potassium channel KCNJ5.
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| Scholl UI, Nelson-Williams C, Yue P, Grekin R, Wyatt RJ, Dillon MJ, Couch R, Hammer LK, Harley FL, Farhi A, Wang WH, Lifton RP.
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| Proc Natl Acad Sci U S A 109(7):2533-8. doi: 10.1073/pnas.1121407109. Epub 2012 Jan 30.
2012
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| 4 | FHA3, KCNJ3, KCNJ5
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| K+ channel mutations in adrenal aldosterone-producing adenomas and hereditary hypertension.
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| Choi M, Scholl UI, Yue P, Björklund P, Zhao B, Nelson-Williams C, Ji W, Cho Y, Patel A, Men CJ, Lolis E, Wisgerhof MV, Geller DS, Mane S, Hellman P, Westin G, Åkerström G, Wang W, Carling T, Lifton RP.
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| Science 331(6018):768-72.
2011
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| 5 | FHA3, KCNJ5
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| Mutations in KCNJ5 gene cause hyperaldosteronism.
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| Zennaro MC, Jeunemaitre X.
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| Circ Res 108(12):1417-8. Review. No abstract available.
2011
|