Page 1/21 Whole Exome Sequencing for the Diagnosis of Rare Genetic Neurodevelopmental Disorders Associated with Cerebellar Atrophy Engy A. Ashaat (  ea.ashaat@nrc.sci.eg ) National Research Centre Hoda A. Ahmed National Research Centre Nesma M. Elaraby National Research Centre Alaaeldin Fayez National Research Centre Ammal M. Metwally National Research Centre Mona K. Mekkawy National Research Centre Neveen A. Ashaat Ain Shams University Rasha Moheb Elhossini National Research Centre Heba Ahmed ElAwady Fayoum University Hospitals Randa H. A. Abdelgawad Ain Shams University Mona El Gammal National Research Centre Mohamed Ahmed Al Kersh Ain Shams University Dina Amin Saleh Ain Shams University Research Article Keywords: Neurodegenerative disorders, Novel variants, Cerebellar atrophy, WES Posted Date: January 19th, 2023 DOI: https://doi.org/10.21203/rs.3.rs-2481124/v1 License:   This work is licensed under a Creative Commons Attribution 4.0 International License. Read Full License