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27. A compound heterozygous mutation in the BSND gene detected in Bartter syndrome type IV. Kitanaka S, Sato U, Maruyama K, Igarashi T. Pediatr Nephrol; 2006 Feb; 21(2):190-3. PubMed ID: 16328537 [Abstract] [Full Text] [Related]
28. Severe manifestation of Bartter syndrome Type IV caused by a novel insertion mutation in the BSND gene. de Pablos AL, García-Nieto V, López-Menchero JC, Ramos-Trujillo E, González-Acosta H, Claverie-Martín F. Clin Nephrol; 2014 May; 81(5):363-8. PubMed ID: 23110775 [Abstract] [Full Text] [Related]
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33. Identification and functional analysis of novel mutations of the CLCNKB gene in Chinese patients with classic Bartter syndrome. Yu Y, Xu C, Pan X, Ren H, Wang W, Meng X, Huang F, Chen N. Clin Genet; 2010 Feb 13; 77(2):155-62. PubMed ID: 19807735 [Abstract] [Full Text] [Related]
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