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A case of pseudohypoaldosteronism type 1 with a mutation in the mineralocorticoid receptor gene
Se Eun Lee, Yun Hye Jung, Kyoung Hee Han, Hyun Kyung Lee, Hee Gyung Kang, Il Soo Ha, Yong Choi, Hae Il Cheong
Clin Exp Pediatr. 2011;54(2):90-93.   Published online February 28, 2011
DOI: https://doi.org/10.3345/kjp.2011.54.2.90

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A case of pseudohypoaldosteronism type 1 with a mutation in the mineralocorticoid receptor gene
Korean Journal of Pediatrics. 2011;54(2):90   Crossref logo
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Mineralocorticoid receptor mutations are the principal cause of renal type 1 pseudohypoaldosteronism
Human Mutation. 2007;28(1):33-40   Crossref logo
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Mutations in the mineralocorticoid receptor gene cause autosomal dominant pseudohypoaldosteronism type I
Nature Genetics. 1998;19(3):279-281   Crossref logo
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Case Reports: Mineralocorticoid-Induced Kaliuresis in Type-II Pseudohypoaldosteronism
The American Journal of the Medical Sciences. 1986;292(4):235-240   Crossref logo
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Molecular characterization of the mineralocorticoid receptor in pseudohypoaldosteronism
Steroids. 1995;60(1):164-167   Crossref logo
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Inactivating mutations of the mineralocorticoid receptor in Type I pseudohypoaldosteronism
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TREATMENT OF MINERALOCORTICOID-RESISTANT RENAL HYPERKALEMIA WITH HYPERTENSION (TYPE II PSEUDOHYPOALDOSTERONISM)
Australian and New Zealand Journal of Medicine. 1986;16(2):221-223   Crossref logo
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Mineralocorticoid-resistant renal hyperkalemia without salt wasting (type II pseudohypoaldosteronism): Role of increased renal chloride reabsorption
Kidney International. 1981;19(5):716-727   Crossref logo
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Novel SCNN1A Gene Splicing-site Mutation Causing Autosomal Recessive Pseudohypoaldosteronism type 1 (PHA1) in two Italian Patients Belonging to the Same Small Town
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A patient with pseudohypoaldosteronism type II caused by a novel mutation in WNK4 gene
Endocrine. 2008;33(3):230-234   Crossref logo
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