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| [1] Anglani FD,Angelo A, Bertizzolo LM, et al. Nephrolithiasis, kidney failure and bone disorders in Dent disease patients with and without CLCN5 mutations[J]. SpringerPlus, 2015, 4(1):492. [2] Pusch M, Zifarelli G. ClC-5: Physiological role and biophysical mechanisms[J]. Cell Calcium, 2015, 58(1):57-66. [3] Wong W, Poke G, Stack M, et al. Phenotypic variability of Dent disease in a large New Zealand kindred[J]. Pediatric Nephrology, 2017, 32(2):1-5. [4] 姚勇. 儿童Dent病及临床相关问题[J]. 中华实用儿科临床杂志, 2018, 33(17):1281-1286. Yaoyong.Dent disease in childhood and associated clinical problems[J]. Chinese Journal of Applied Clinical Pediatrics, 2018, 33(17):1281-1286. [5] Van Berkel Y, Ludwig M, van Wijk J.A.E, et al. Proteinuria in Dent disease: a review of the literature[J]. Pediatric Nephrology, 2017, 32(10): 1851-1859. [6] Mansour-Hendili L, Blanchard A, Le Pottier N, et al. Mutation Update of the\r, CLCN5\r, Gene Responsible for Dent Disease 1[J]. Human Mutation, 2015, 36(8):743-752. [7] Zhang H, Wang F, Xiao H, et al. Dent disease: Same CLCN5 mutation but different phenotypes in two brothers in China[J]. Intractable & Rare Diseases Research, 2017, 6(2):114-118. [8] 张宏博. 儿童Dent病研究进展[J]. 中国实用儿科杂志, 2015, 30(1): 77-80. ZHANG Hongbo. Latest research progress in childhood Dent disease[J]. Chinese Journal of Practical Pediatrics, 2015, 30(1): 77-80. |
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