1. Lu, Yiting, Liu, Xinchang, Sun, Lin, Liu, Yaxin, Zhou, Xianliang. 2023. A frameshift mutation in the SCNN1B gene in a family with Liddle syndrome: A case report and systematic review. In Molecular medicine reports, 29, . doi:10.3892/mmr.2023.13142. https://pubmed.ncbi.nlm.nih.gov/38099339/
2. Stanke, Frauke, Becker, Tim, Ismer, Haide Susanne, Dittrich, Anna-Maria, Tümmler, Burkhard. 2021. Consistent Assignment of Risk and Benign Allele at rs2303153 in the CF Modifier Gene SCNN1B in Three Independent F508del-CFTR Homozygous Patient Populations. In Genes, 12, . doi:10.3390/genes12101554. https://pubmed.ncbi.nlm.nih.gov/34680949/
3. Joshi, Kamal, Verma, Prashant Kumar, Barman, Manidipa. 2022. Systemic Pseudohypoaldosteronism Type 1 Due to a Novel Mutation in SCNN1B Gene: A Case Report. In EJIFCC, 33, 268-273. doi:. https://pubmed.ncbi.nlm.nih.gov/36447799/
4. Becker, Tim, Pich, Andreas, Tamm, Stephanie, Tümmler, Burkhard, Stanke, Frauke. 2020. Genetic information from discordant sibling pairs points to ESRP2 as a candidate trans-acting regulator of the CF modifier gene SCNN1B. In Scientific reports, 10, 22447. doi:10.1038/s41598-020-79804-y. https://pubmed.ncbi.nlm.nih.gov/33384439/
5. Zhong, Qilong, Liu, Chunyan, Fan, Rui, Yin, Fengying, Zhang, Lina. 2016. Association of SCNN1B promoter methylation with essential hypertension. In Molecular medicine reports, 14, 5422-5428. doi:10.3892/mmr.2016.5905. https://pubmed.ncbi.nlm.nih.gov/27840946/
6. Qian, Yun, Zhou, Lianxin, Luk, Simson Tsz Yat, Yu, Jun, Wong, Chi Chun. 2022. The sodium channel subunit SCNN1B suppresses colorectal cancer via suppression of active c-Raf and MAPK signaling cascade. In Oncogene, 42, 601-612. doi:10.1038/s41388-022-02576-4. https://pubmed.ncbi.nlm.nih.gov/36564468/
7. Nobel, Yael R, Lodish, Maya B, Raygada, Margarita, Stratakis, Constantine A, Zilbermint, Mihail. 2016. Pseudohypoaldosteronism type 1 due to novel variants of SCNN1B gene. In Endocrinology, diabetes & metabolism case reports, 2016, 150104. doi:10.1530/EDM-15-0104. https://pubmed.ncbi.nlm.nih.gov/26807262/
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