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…

Overview of attention for article published in BMC Nephrology, July 2018

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novel CLDN16 mutation https://t.co/dhh3ZNHLlk in #Chinese patient with Familial hypomagnesaemia, Hypercalciuria and Nephrocalcinosis #KidneyDisease https://t.co/c7bGGPCpcJ

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