Accepted Manuscript Biallelic mutations in AP3D1 cause Hermansky-Pudlak syndrome type 10 associated with immunodeficiency and seizure disorder Mohammed Mohammed, Nadia Al-Hashmi, Samiya Al-Rashdi, Nashat Al-Sukaiti, Kawther Al-Adawi, Marwa Al-Riyami, Almundher Al-Maawali PII: S1769-7212(18)30598-6 DOI: https://doi.org/10.1016/j.ejmg.2018.11.017 Reference: EJMG 3583 To appear in: European Journal of Medical Genetics Received Date: 8 August 2018 Revised Date: 5 November 2018 Accepted Date: 22 November 2018 Please cite this article as: M. Mohammed, N. Al-Hashmi, S. Al-Rashdi, N. Al-Sukaiti, K. Al-Adawi, M. Al-Riyami, A. Al-Maawali, Biallelic mutations in AP3D1 cause Hermansky-Pudlak syndrome type 10 associated with immunodeficiency and seizure disorder, European Journal of Medical Genetics (2018), doi: https://doi.org/10.1016/j.ejmg.2018.11.017. 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.