Accepted Manuscript Progressive myoclonus epilepsy and ceroidolipofuscinosis 14: The multifaceted phenotypic spectrum of KCTD7-RELATED disorders Mario Mastrangelo, Stefano Sartori, Alessandro Simonati, Mario Brinciotti, Francesca Moro, Margherita Nosadini, Francesco Pezzini, Stefano Doccini, Filippo Maria Santorelli, Vincenzo Leuzzi PII: S1769-7212(18)30404-X DOI: https://doi.org/10.1016/j.ejmg.2018.11.025 Reference: EJMG 3591 To appear in: European Journal of Medical Genetics Received Date: 31 May 2018 Revised Date: 28 September 2018 Accepted Date: 22 November 2018 Please cite this article as: M. Mastrangelo, S. Sartori, A. Simonati, M. Brinciotti, F. Moro, M. Nosadini, F. Pezzini, S. Doccini, F.M. Santorelli, V. Leuzzi, Progressive myoclonus epilepsy and ceroidolipofuscinosis 14: The multifaceted phenotypic spectrum of KCTD7-RELATED disorders, European Journal of Medical Genetics (2018), doi: https://doi.org/10.1016/j.ejmg.2018.11.025. This is a PDF file of an unedited manuscript that has been accepted for publication. As a service to our customers we are providing this early version of the manuscript. The manuscript will undergo copyediting, typesetting, and review of the resulting proof before it is published in its final form. Please note that during the production process errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal pertain.