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

European Journal of Human Genetics, Published online: 10 September 2019; doi:10.1038/s41431-019-0491-5Correction: Phenotypic spectrum associated with a CRADD founder variant underlying frontotemporal predominant pachygyria in the Finnish population

Source: European Journal of Human Genetics - September 9, 2019 Category: Genetics & Stem Cells Authors: Daniel L. Polla Elisa Rahikkala Michaela K. Bode Tuomo M äättä Teppo Varilo Thyrza Loman Anju K. Philips Mitja Kurki Aarno Palotie Jarmo K örkkö P äivi Vieira Kristiina Avela Val érie Jacquemin Isabelle Pirson Marc Abramowicz Arjan P. M. de Brouwer Source Type: research