Lu, J., Zhao, X., Paiardini, A., Lang, Y., Bottillo, I., & Shao, L. (2018). Familial hypomagnesaemia, Hypercalciuria and Nephrocalcinosis associated with a novel mutation of the highly conserved leucine residue 116 of Claudin 16 in a Chinese patient with a delayed diagnosis: A case report. BMC Nephrol.

Lu, Jingru, Xiangzhong Zhao, Alessandro Paiardini, Yanhua Lang, Irene Bottillo, and Leping Shao. "Familial Hypomagnesaemia, Hypercalciuria and Nephrocalcinosis Associated With a Novel Mutation of the Highly Conserved Leucine Residue 116 of Claudin 16 in a Chinese Patient With a Delayed Diagnosis: A Case Report." BMC Nephrol 2018.

Lu, Jingru, et al. "Familial Hypomagnesaemia, Hypercalciuria and Nephrocalcinosis Associated With a Novel Mutation of the Highly Conserved Leucine Residue 116 of Claudin 16 in a Chinese Patient With a Delayed Diagnosis: A Case Report." BMC Nephrol 2018.