Amelogenesis imperfecta in familial hypomagnesaemia and hypercalciuria with nephrocalcinosis caused by CLDN19 gene mutations
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| Description | scientific article |
| Author/s |
author: Ariane Berdal Muriel de la Dure Molla Jean-Christophe Fricain Maria do Carmo Scher Paulo Marcio Yamaguti Catherine Chaussain Sylvie Babajko Renaud de La Faille Ana Carolina Acevedo Marie-Lucile Figueres Maristela Estevão Barbosa Luiz Claudio Castro |
| Publication date | August 16, 2016 |
| Language | English |
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