1. Yun, Yejin, Park, Sang Soo, Lee, Soyoung, Park, Seongyeol, Lee, Sang-Yeon. 2023. Expanding Genotype-Phenotype Correlation of CLCNKA and CLCNKB Variants Linked to Hearing Loss. In International journal of molecular sciences, 24, . doi:10.3390/ijms242317077. https://pubmed.ncbi.nlm.nih.gov/38069401/
2. Mrad, Flavia Cristina Carvalho, Soares, Sílvia Bouissou Morais, de Menezes Silva, Luiz Alberto Wanderley, Dos Anjos Menezes, Pedro Versiani, Simões-E-Silva, Ana Cristina. 2020. Bartter's syndrome: clinical findings, genetic causes and therapeutic approach. In World journal of pediatrics : WJP, 17, 31-39. doi:10.1007/s12519-020-00370-4. https://pubmed.ncbi.nlm.nih.gov/32488762/
3. Barlassina, Cristina, Dal Fiume, Chiara, Lanzani, Chiara, Macciardi, Fabio, Cusi, Daniele. 2007. Common genetic variants and haplotypes in renal CLCNKA gene are associated to salt-sensitive hypertension. In Human molecular genetics, 16, 1630-8. doi:. https://pubmed.ncbi.nlm.nih.gov/17510212/
4. Tavira, Beatriz, Gómez, Juan, Santos, Fernando, Alvarez, Victoria, Coto, Eliecer. 2014. A labor- and cost-effective non-optical semiconductor (Ion Torrent) next-generation sequencing of the SLC12A3 and CLCNKA/B genes in Gitelman's syndrome patients. In Journal of human genetics, 59, 376-80. doi:10.1038/jhg.2014.37. https://pubmed.ncbi.nlm.nih.gov/24830959/
5. Cappola, Thomas P, Matkovich, Scot J, Wang, Wei, Nerbonne, Jeanne M, Dorn, Gerald W. 2011. Loss-of-function DNA sequence variant in the CLCNKA chloride channel implicates the cardio-renal axis in interindividual heart failure risk variation. In Proceedings of the National Academy of Sciences of the United States of America, 108, 2456-61. doi:10.1073/pnas.1017494108. https://pubmed.ncbi.nlm.nih.gov/21248228/