1. Elfert, Khaled A, Geller, David S, Nelson-Williams, Carol, Al-Malki, Hassan, Nauman, Awais. 2020. Late-Onset Bartter Syndrome Type II Due to a Homozygous Mutation in KCNJ1 Gene: A Case Report and Literature Review. In The American journal of case reports, 21, e924527. doi:10.12659/AJCR.924527. https://pubmed.ncbi.nlm.nih.gov/32997650/
2. Li, Jingyi, Hu, Shoulong, Nie, Yi, Li, Hongmei, Zhu, Shuanli. . A novel compound heterozygous KCNJ1 gene mutation presenting as late-onset Bartter syndrome: Case report. In Medicine, 98, e16738. doi:10.1097/MD.0000000000016738. https://pubmed.ncbi.nlm.nih.gov/31441846/
3. Tian, Mi, Peng, Hui, Bi, Xin, Wu, Yan, Zhang, Bei-Ru. 2022. Late-Onset Bartter Syndrome Type II Due to a Novel Compound Heterozygous Mutation in KCNJ1 Gene: A Case Report and Literature Review. In Frontiers in medicine, 9, 862514. doi:10.3389/fmed.2022.862514. https://pubmed.ncbi.nlm.nih.gov/35463019/
4. Cogal, Andrea G, Arroyo, Jennifer, Shah, Ronak Jagdeep, Lieske, John C, Harris, Peter C. 2021. Comprehensive Genetic Analysis Reveals Complexity of Monogenic Urinary Stone Disease. In Kidney international reports, 6, 2862-2884. doi:10.1016/j.ekir.2021.08.033. https://pubmed.ncbi.nlm.nih.gov/34805638/
5. Gaggar, Payal, Raju, D Sree Bhushan, Tej, M Ravi, Pragna, P. 2022. Late-Onset Bartter's Syndrome Type II with End-Stage Renal Disease Due to a Novel Mutation in KCNJ1 Gene in an Indian Adult Male - A Case Report. In Indian journal of nephrology, 33, 57-60. doi:10.4103/ijn.ijn_383_21. https://pubmed.ncbi.nlm.nih.gov/37197039/
6. Guo, Zhongqiang, Liu, Jin, Zhang, Lian, Li, Xuesong, Zhou, Liqun. 2014. KCNJ1 inhibits tumor proliferation and metastasis and is a prognostic factor in clear cell renal cell carcinoma. In Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine, 36, 1251-9. doi:10.1007/s13277-014-2746-7. https://pubmed.ncbi.nlm.nih.gov/25344677/
7. Hebert, Steven C. . Bartter syndrome. In Current opinion in nephrology and hypertension, 12, 527-32. doi:. https://pubmed.ncbi.nlm.nih.gov/12920401/
8. Zuo, Jianxin, Guo, Wencong, Wang, Shujuan, Han, Yue, Shao, Leping. 2020. Eight novel KCNJ1 variants and parathyroid hormone overaction or resistance in 5 probands with Bartter syndrome type 2. In Clinica chimica acta; international journal of clinical chemistry, 511, 248-254. doi:10.1016/j.cca.2020.10.002. https://pubmed.ncbi.nlm.nih.gov/33058840/
9. Mani, Srinivasan, Nair, Jayasree, Handa, Deepali. 2021. Antenatal Bartter syndrome: a new compound heterozygous mutation in exon 2 of KCNJ1 gene. In BMJ case reports, 14, . doi:10.1136/bcr-2021-244685. https://pubmed.ncbi.nlm.nih.gov/34663630/
10. Yang, Saisai, Yao, Guanghui, Chen, Xin, Kong, Xiangdong, Wu, Qinghua. 2022. A novel mutation of KCNJ1 identified in an affected child with nephrolithiasis. In BMC nephrology, 23, 227. doi:10.1186/s12882-022-02783-x. https://pubmed.ncbi.nlm.nih.gov/35761198/
智鼠故事 
