reference/8006136

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/8006136

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endingPage	260
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bibliographicCitation	Xekouki P, Hatch MM, Lin L, Rodrigo de A, Azevedo M, de la Luz Sierra M, Levy I, Saloustros E, Moraitis A, Horvath A, Kebebew E, Hoffman DA, Stratakis CA. KCNJ5 mutations in the National Institutes of Health cohort of patients with primary hyperaldosteronism: an infrequent genetic cause of Conn's syndrome. Endocr Relat Cancer. 2012 Jun;19(3):255–60. PMID: 22323562; PMCID: PMC4041522.
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date	201206
identifier	https://pubmed.ncbi.nlm.nih.gov/PMC4041522 https://pubmed.ncbi.nlm.nih.gov/22323562 https://doi.org/10.1530/erc-12-0022
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	KCNJ5 mutations in the National Institutes of Health cohort of patients with primary hyperaldosteronism: an infrequent genetic cause of Conn's syndrome
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