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. 2019 Sep 10;28(4):532. doi: 10.1038/s41431-019-0491-5

Correction: Phenotypic spectrum associated with a CRADD founder variant underlying frontotemporal predominant pachygyria in the Finnish population

Daniel L Polla 1,2,#, Elisa Rahikkala 3,#, Michaela K Bode 4,#, Tuomo Määttä 5, Teppo Varilo 6, Thyrza Loman 1, Anju K Philips 6, Mitja Kurki 7,8,9, Aarno Palotie 7,8,9,10,11, Jarmo Körkkö 12, Päivi Vieira 13, Kristiina Avela 14, Valérie Jacquemin 15, Isabelle Pirson 15, Marc Abramowicz 15, Arjan P M de Brouwer 1, Outi Kuismin 3,9, Hans van Bokhoven 1,#, Irma Järvelä 6,✉,#
PMCID: PMC7080772  PMID: 31506600

Correction to:European Journal of Human Genetics

10.1038/s41431-019-0383-8

Published online 26 March 2019

Post-publication the authors realised they had accidently omitted Dr. Päivi Vieira’s name from the author list. Dr. Vieira from the Clinic for Children and Adolescents, PEDEGO Research Unit and Medical Research Center Oulu, Oulu University Hospital and University of Oulu, Finland, participated in the collaborative work describing CRADD-founder mutation in the Finnish population. She also provided and interpreted clinical data to Table and Supplements and interpreted the EEG-findings that are present in this manuscript. Dr. Vieira has now been included in the original manuscript.

Articles from European Journal of Human Genetics are provided here courtesy of Nature Publishing Group

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