Associated Papers
A novel mutation in CLDN16 results in rare familial hypomagnesaemia with hypercalciuria and nephrocalcinosis in a Chinese family.
Lv F et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry, 2016
Unusual clinical presentation and possible rescue of a novel claudin-16 mutation.
Müller D et al.
The Journal of Clinical Endocrinology and Metabolism, 2006
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