Additional file 1 of Clinical and genetic heterogeneity of syndromic hearing loss and its non-syndromic hearing loss mimics
Asuman Koparir(University of Würzburg), Barbara Vona(Brigham and Women's Hospital), Tobias B. Haack(Technical University of Munich), Stefanie Tovornik(University of Würzburg), Michaela A. H. Hofrichter(University of Würzburg), Mohsen Rajati(Mashhad University of Medical Sciences), Stephen Loum(University of Tübingen), Shahrooz Ghaderi(Universitätsmedizin Göttingen), Mohammad Doosti, Julia Doll(University of Würzburg), Tayebeh Baranzehi, Dor Mohammad Kordi-Tamandani(University of Sistan and Baluchestan), Madiha Shadab(Mirpur University of Science and Technology), Erkan Koparir(University of Würzburg), Ansar Ahmed Abbasi(University of Azad Jammu and Kashmir), Paola Cisneros Linares(Universidad Nacional Autónoma de México), Shahryar Alavi(National Hospital for Neurology and Neurosurgery), Erdmute Kunstmann, İrem Kalay(Ümraniye Eğitim ve Araştırma Hastanesi), Nele Christophersen(Universitätsmedizin Göttingen), Niloofar Chamanrou(Shahrekord University), Daniel Owrang(German Primate Center), Sophie Flandin, Hannie Kremer(Radboud University Nijmegen), Rahema Mohammad(National Hospital for Neurology and Neurosurgery), Daniel Villalobos(University of Würzburg), Maryam Naghinejad(Tabriz University of Medical Sciences), Aboulfazl Rad(Sabzevar University of Medical Sciences), Mina Zamini(Shahid Chamran University of Ahvaz), Paulina Bahena Carbajal(University of Würzburg), Neda Dragicevic Babic(Universitätsklinikum Würzburg), Hamid Galehdari(Shahid Chamran University of Ahvaz), Reza Maroofian, David J. Murphy, Luis Nicolás Martínez Völter(German Primate Center), Henry Houlden, Wafaa Shehata-Dieler, Thomas Haaf(University of Würzburg), Paria Najarzadeh Torbati, Neda Alidadiani, Ehsan Ghayoor Karimiani, Helge Hebestreit(Universitätsklinikum Würzburg)
Cited by 0
Related Papers
Loss-of-function mutations in MGME1 impair mtDNA replication and cause multisystemic mitochondrial disease
|Nature Genetics|2013|237
Mutations in FBXL4, Encoding a Mitochondrial Protein, Cause Early-Onset Mitochondrial Encephalomyopathy
|The American Journal of Human Genetics|2013|181
Mutations in GTPBP3 Cause a Mitochondrial Translation Defect Associated with Hypertrophic Cardiomyopathy, Lactic Acidosis, and Encephalopathy
|The American Journal of Human Genetics|2014|157
SYT1-associated neurodevelopmental disorder: a case series
|Brain|2018|143