Maria C. Scher
Brasilia, DF, Brazil
Last Updated: 09/26/2026
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Found 1 publications
Amelogenesis imperfecta in familial hypomagnesaemia and hypercalciuria with nephrocalcinosis caused by CLDN19 gene mutations.
Journal: Journal of medical genetics
Published: May 11, 2016
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Last Updated: 09/26/2026