Article Text

other Versions

PDF

Correction: Amelogenesis imperfecta in familial hypomagnesaemia and hypercalciuria with nephrocalcinosis caused by CLDN19 gene mutations

Statistics from Altmetric.com

Yamaguti PM, Neves FDAR, Hotton D, et al. Amelogenesis imperfecta in familial hypomagnesaemia and hypercalciuria with nephrocalcinosis caused by CLDN19 gene mutations. J Med Genet 2017;54:26–37.

One of the author names is spelled incorrectly. ‘Pascal Houiller’ should be ‘Pascal Houillier’.

View Abstract

Request permissions

If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.

Linked Articles

  • Genotype-phenotype correlations
    Paulo Marcio Yamaguti Francisco de Assis Rocha Neves Dominique Hotton Claire Bardet Muriel de La Dure-Molla Luiz Claudio Castro Maria do Carmo Scher Maristela Estevão Barbosa Christophe Ditsch Jean-Christophe Fricain Renaud de La Faille Marie-Lucile Figueres Rosa Vargas-Poussou Pascal Houiller Catherine Chaussain Sylvie Babajko Ariane Berdal Ana Carolina Acevedo J Hou C Klein K Jedeon