PT - JOURNAL ARTICLE ED - , TI - <em>Correction: Amelogenesis imperfecta in familial hypomagnesaemia and hypercalciuria with nephrocalcinosis caused by CLDN19 gene mutations</em> AID - 10.1136/jmedgenet-2016-103956corr1 DP - 2017 Sep 25 TA - Journal of Medical Genetics PG - e103956corr1 4099 - http://jmg.bmj.com/content/early/2017/09/24/jmedgenet-2016-103956corr1.short 4100 - http://jmg.bmj.com/content/early/2017/09/24/jmedgenet-2016-103956corr1.full