Article info
Genotype-phenotype correlations
Original article
Amelogenesis imperfecta in familial hypomagnesaemia and hypercalciuria with nephrocalcinosis caused by CLDN19 gene mutations
- Correspondence to Dr Ana Carolina Acevedo; University of Brasilia, University Hospital of Brasilia, Oral Center for Inherited Diseases, Brasilia CEP:70372-050, Brazil; acevpoppe{at}gmail.com
Citation
Amelogenesis imperfecta in familial hypomagnesaemia and hypercalciuria with nephrocalcinosis caused by CLDN19 gene mutations
Publication history
- Received May 11, 2016
- Revised July 15, 2016
- Accepted July 27, 2016
- First published August 16, 2016.
Online issue publication
December 14, 2016
Article Versions
- Previous version (16 August 2016).
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