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Trans Assoc Am Physicians 76: 199\u2013213."},{"key":"2","doi-asserted-by":"crossref","unstructured":"2 Mori T, Hosomichi K, Chiga M, Mandai S, Nakaoka H, et al. (2017) Comprehensive genetic testing approach for major inherited kidney diseases, using next-generation sequencing with a custom panel. Clin Exp Nephrol 21: 63\u201375.","DOI":"10.1007\/s10157-016-1252-1"},{"key":"3","doi-asserted-by":"crossref","unstructured":"3 Burrello J, Monticone S, Buffolo F, Tetti M, Veglio F, et al. (2017) Is there a role for genomics in the management of hypertension? Int J Mol Sci 18: 1131\u20131147.","DOI":"10.3390\/ijms18061131"},{"key":"4","doi-asserted-by":"crossref","unstructured":"4 Levanovich PE, Diaczok A, Rossi NF (2020) Clinical and molecular perspectives monogenic hypertension. Curr Hypertens Rev 16: 91\u2013107.","DOI":"10.2174\/1573402115666190409115330"},{"key":"5","doi-asserted-by":"crossref","unstructured":"5 Fan P, Pan XC, Zhang D, Yang KQ, Zhang Y, et al. (2020) Pediatric Liddle syndrome caused by a novel <i>SCNN1G<\/i> variant in a Chinese family and characterized by early-onset hypertension. Am J Hypertens 33: 670\u2013675.","DOI":"10.1093\/ajh\/hpaa037"},{"key":"6","doi-asserted-by":"crossref","unstructured":"6 Wang LP, Yang KQ, Jiang XJ, Wu HY, Zhang HM, et al. (2015) Prevalence of Liddle syndrome among young hypertension patients of undetermined cause in Chinese population. J Clin Hypertens (Greenwich) 17: 902\u2013907.","DOI":"10.1111\/jch.12598"},{"key":"7","doi-asserted-by":"crossref","unstructured":"7 Liu K, Qin F, Sun X, Zhang Y, Wang J, et al. (2018) Analysis of the genes involved in Mendelian forms of low-renin hypertension in Chinese early-onset hypertensive patients. J Hypertens 36: 502\u2013509.","DOI":"10.1097\/HJH.0000000000001556"},{"key":"8","doi-asserted-by":"crossref","unstructured":"8 Polfus LM, Boerwinkle E, Gibbs RA, Metcalf G, Muzny D, et al. (2016) Whole-exome sequencing reveals an inherited R566X mutation of the epitheral sodium channel \u03b2-subunit in a case of early-onset phenotype of Liddle syndrome. Cold Spring Harb Mol Case Stud 2: a001255.","DOI":"10.1101\/mcs.a001255"},{"key":"9","doi-asserted-by":"publisher","unstructured":"9 Shimkets RA, Warnock DG, Bositis CM, Nelson-Williams C, Hansson JH, et al. (1994) Liddle\u2019s syndrome: heritable human hypertension caused by mutations in the subunit of the epithelial sodium channel. Cell 79: 407\u2013414.","DOI":"10.1016\/0092-8674(94)90250-X"},{"key":"10","doi-asserted-by":"publisher","unstructured":"10 Melander O, Orho M, Fagerudd J, Bengtsson K, Groop PH, et al. (1998) Mutations and variants of the epithelial sodium channel gene in Liddle\u2019s syndrome and primary hypertension. 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(2022) Liddle syndrome misdiagnosed as primary aldosteronism is caused by inaccurate aldosterone-rennin detection while a novel <i>SCNN1G<\/i> mutation is discovered. Blood Press 31: 139\u2013145.","DOI":"10.1080\/08037051.2022.2088471"},{"key":"15","doi-asserted-by":"crossref","unstructured":"15 Funder JW, Carey RM, Mantero F, Murad MH, Reincke M, et al. (2016) The management of primary aldosteronism: case detection, diagnosis, and treatment: an Endocrine Society clinical practice guideline. J Clin Endocrinol Metab 101: 1889\u20131916.","DOI":"10.1210\/jc.2015-4061"},{"key":"16","doi-asserted-by":"crossref","unstructured":"16 Stowasser M, Ahmed A, Pimenta E, Taylor P, Gordon R (2011) Factors affecting the aldosterone\/renin ratio. Horm Metab Res 44: 170\u2013176.","DOI":"10.1055\/s-0031-1295460"},{"key":"17","doi-asserted-by":"crossref","unstructured":"17 Naruse M, Katabami T, Shibata H, Sone M, Takahashi K, et al. 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