دورية أكاديمية

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

التفاصيل البيبلوغرافية
العنوان: 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
المؤلفون: Lu, JingruAff1, Aff2, Zhao, Xiangzhong, Paiardini, Alessandro, Lang, Yanhua, Bottillo, Irene, Shao, LepingAff1, Aff2
المصدر: BMC Nephrology. 19(1)
قاعدة البيانات: Springer Nature Journals
الوصف
تدمد:14712369
DOI:10.1186/s12882-018-0979-1