Cite
HARVARD Citation
Yamaguti, P. et al. (2017). Amelogenesis imperfecta in familial hypomagnesaemia and hypercalciuria with nephrocalcinosis caused by CLDN19 gene mutations. Journal of medical genetics. 54 (1), pp. 26-37. [Online].
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Yamaguti, P. et al. (2017). Amelogenesis imperfecta in familial hypomagnesaemia and hypercalciuria with nephrocalcinosis caused by CLDN19 gene mutations. Journal of medical genetics. 54 (1), pp. 26-37. [Online].