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. 2020 Sep 3;107(3):580. doi: 10.1016/j.ajhg.2020.08.004

Loss of Function of RIMS2 Causes a Syndromic Congenital Cone-Rod Synaptic Disease with Neurodevelopmental and Pancreatic Involvement

Sabrina Mechaussier, Basamat Almoallem, Christina Zeitz, Kristof Van Schil, Laila Jeddawi, Jo Van Dorpe, Alfredo Dueñas Rey, Christel Condroyer, Olivier Pelle, Michel Polak, Nathalie Boddaert, Nadia Bahi-Buisson, Mara Cavallin, Jean-Louis Bacquet, Alexandra Mouallem-Bézière, Olivia Zambrowski, José Alain Sahel, Isabelle Audo, Josseline Kaplan, Jean-Michel Rozet, Elfride De Baere ∗∗, Isabelle Perrault ∗
PMCID: PMC7477002  PMID: 32888510

(The American Journal of Human Genetics 106, 859–871; June 4, 2020)

In the originally published version of this article, the accession number given for RIMS2α was incorrect. It should have been NM_001348484.1. The number has now been corrected online. The authors regret the error.

Contributor Information

Elfride De Baere, Email: elfride.debaere@ugent.be.

Isabelle Perrault, Email: isabelle.perrault@inserm.fr.

Articles from American Journal of Human Genetics are provided here courtesy of American Society of Human Genetics

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