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Elucidating the underlying molecular pathogenesis of NR3C2 mutants causing autosomal dominant pseudohypoaldosteronism type 1.
J Clin Endocrinol Metab. 2006 Nov;91(11):4552-61. doi: 10.1210/jc.2006-1161. Epub 2006 Sep 5.
J Clin Endocrinol Metab. 2006.
PMID: 16954160
Autosomal dominant pseudohypoaldosteronism type 1: mechanisms, evidence for neonatal lethality, and phenotypic expression in adults.
Geller DS, Zhang J, Zennaro MC, Vallo-Boado A, Rodriguez-Soriano J, Furu L, Haws R, Metzger D, Botelho B, Karaviti L, Haqq AM, Corey H, Janssens S, Corvol P, Lifton RP.
Geller DS, et al.
J Am Soc Nephrol. 2006 May;17(5):1429-36. doi: 10.1681/ASN.2005111188. Epub 2006 Apr 12.
J Am Soc Nephrol. 2006.
PMID: 16611713
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