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Pseudohypoaldosteronism in a newborn male with functional polymorphisms in the mineralocorticoid receptor genes
Hyun Ah Jeong, Yoon Kyoung Park, Yeong Sang Jung, Myung-Hyun Nam, Hyo-Kyoung Nam, Kee Hyoung Lee, Young-Jun Rhie
Ann Pediatr Endocrinol Metab. 2015;20(4):230-234.   Published online December 31, 2015
DOI: https://doi.org/10.6065/apem.2015.20.4.230

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Pseudohypoaldosteronism in a newborn male with functional polymorphisms in the mineralocorticoid receptor genes
Annals of Pediatric Endocrinology & Metabolism. 2015;20(4):230   Crossref logo
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Functional polymorphisms in the mineralocorticoid receptor and amirolide-sensitive sodium channel genes in a patient with sporadic pseudohypoaldosteronism
Human Genetics. 2003;112(1):91-97   Crossref logo
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Molecular characterization of the mineralocorticoid receptor in pseudohypoaldosteronism
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Mutations and Polymorphisms, and Their Functional Consequences, in Gonadotropin and Gonadotropin Receptor Genes
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Pseudohypoaldosteronism Type 1 due to a Novel Mutation in the Mineralocorticoid Receptor Gene
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Mineralocorticoid receptor mutations are the principal cause of renal type 1 pseudohypoaldosteronism
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