Mutations in EPG5 are associated with a wide spectrum of neurodevelopmental and neurodegenerative disorders
Hormos Salimi Dafsari(University of Cologne), Sheela Nampoothiri(Amrita Institute of Medical Sciences and Research Centre), Felix Distelmaier(Düsseldorf University Hospital), Carrie Mohila(Baylor College of Medicine), Haidar S. Dafsari(University of Cologne), Suvasini Sharma(University of Delhi), Celine Deneubourg(Johnson & Johnson (United States)), Dora Steel(Great Ormond Street Hospital), Saurabh Chopra(Medanta The Medicity), Ay Lin Kho(King's College London), Mina Zamani(Shahid Chamran University of Ahvaz), Andrew Fennell(Monash Health), Bernice Lo(Qatar Airways (Qatar)), Dana Marafi(Kuwait University), Erika Beckman(Seattle Children's Hospital), Daniel G. Calame, Saeid Sadeghian(Ahvaz Jundishapur University of Medical Sciences), Darius Ebrahimi‐Fakhari(Boston Children's Hospital), Ata Siddiqui(King's College Hospital), Alireza Sedaghat(Ahvaz Jundishapur University of Medical Sciences), Ruizhi Duan(Baylor College of Medicine), Anthony Lang(University Health Network), Frances Elmslie(St George’s University Hospitals NHS Foundation Trust), Martina Baethmann, Jawaher Zeighami, Karen P. Steel(King's College London), Luisa Averdunk(Düsseldorf University Hospital), Hamid Galehdari(Shahid Chamran University of Ahvaz), Afshin Saffari(Heidelberg University), Nicolai Kohlschmidt(University of Zurich), Büşra Eser Çavdartepe(Konya Eğitim ve Araştırma Hastanesi), Steffi Patzer(Krankenhaus St. Elisabeth und St. Barbara), Reza Azizi Malamiri(Ahvaz Jundishapur University of Medical Sciences), Alice Abdel Aleem(National Research Centre), Reza Maroofian(University College London), Kairit Joost(University of Tartu), Gholamreza Shariati(Ahvaz Jundishapur University of Medical Sciences), Birgit Gerisch(Max Planck Institute for Biology of Ageing), Irene J. Chang(Seattle Children's Hospital), Lea Hentrich(University of Cologne), Franciska Baur(University of Cologne), Zita Suprenant(Rome Foundation), Michael Harris(Rome Foundation), Mehri Salari(Shahid Beheshti University of Medical Sciences), Cesar Alvares(Boston Children's Hospital), Adrian Boehnke(Baylor College of Medicine), Renate Peters(University Hospital of Wales), Neil J. Ingham(King's College London), Kritarth Singh(University College London), Preethi Sheshadri(University College London)
Cited by 4
Related Papers
Immune dysregulation in human subjects with heterozygous germline mutations in <i>CTLA4</i>
|Science|2014|844
Identification of diverse astrocyte populations and their malignant analogs
|Nature Neuroscience|2017|532
Mutations in INPP5E, encoding inositol polyphosphate-5-phosphatase E, link phosphatidyl inositol signaling to the ciliopathies
|Nature Genetics|2009|412
Distinct Roles<i>In Vivo</i>for the Ubiquitin–Proteasome System and the Autophagy–Lysosomal Pathway in the Degradation of α-Synuclein
|Journal of Neuroscience|2011|373
Levodopa Dose Equivalency in Parkinson's Disease: Updated Systematic Review and Proposals
|Movement Disorders|2023|351