1. García-Nieto, Víctor, Flores, Carlos, Luis-Yanes, Maria I, Villar, Jesús, Claverie-Martín, Félix. 2006. Mutation G47R in the BSND gene causes Bartter syndrome with deafness in two Spanish families. In Pediatric nephrology (Berlin, Germany), 21, 643-8. doi:. https://pubmed.ncbi.nlm.nih.gov/16572343/
2. Kitanaka, Sachiko, Sato, Utako, Maruyama, Kenichi, Igarashi, Takashi. 2005. A compound heterozygous mutation in the BSND gene detected in Bartter syndrome type IV. In Pediatric nephrology (Berlin, Germany), 21, 190-3. doi:. https://pubmed.ncbi.nlm.nih.gov/16328537/
3. Birkenhäger, R, Otto, E, Schürmann, M J, Kispert, A, Hildebrandt, F. . Mutation of BSND causes Bartter syndrome with sensorineural deafness and kidney failure. In Nature genetics, 29, 310-4. doi:. https://pubmed.ncbi.nlm.nih.gov/11687798/
4. Hayama, Atsushi, Rai, Tatemitsu, Sasaki, Sei, Uchida, Shinichi. 2003. Molecular mechanisms of Bartter syndrome caused by mutations in the BSND gene. In Histochemistry and cell biology, 119, 485-93. doi:. https://pubmed.ncbi.nlm.nih.gov/12761627/
5. Elrharchi, Soukaina, Riahi, Zied, Salime, Sara, Petit, Christine, Barakat, Abdelhamid. 2018. Two novel homozygous missense mutations identified in the BSND gene in Moroccan patients with Bartter's syndrome. In International journal of pediatric otorhinolaryngology, 113, 46-50. doi:10.1016/j.ijporl.2018.07.010. https://pubmed.ncbi.nlm.nih.gov/30174009/
6. de Pablos, Augusto Luque, García-Nieto, Victor, López-Menchero, Jesús C, González-Acosta, Hilaria, Claverie-Martín, Félix. . Severe manifestation of Bartter syndrome Type IV caused by a novel insertion mutation in the BSND gene. In Clinical nephrology, 81, 363-8. doi:10.5414/CN107687. https://pubmed.ncbi.nlm.nih.gov/23110775/
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