RT Journal Article SR Electronic T1 Correction: Amelogenesis imperfecta in familial hypomagnesaemia and hypercalciuria with nephrocalcinosis caused by CLDN19 gene mutations JF Journal of Medical Genetics JO J Med Genet FD BMJ Publishing Group Ltd SP e103956corr1 DO 10.1136/jmedgenet-2016-103956corr1 YR 2017 UL http://jmg.bmj.com/content/early/2017/09/24/jmedgenet-2016-103956corr1.abstract AB