Genotype-Phenotype Correlations in Charcot-Marie-Tooth Disease Due to MTMR2 Mutations and Implications in Membrane Trafficking
Haicui Wang(Hong Kong Polytechnic University), Sebahattin Çırak(University of Cologne), Mehmet Yaşar(Kayseri Eğitim ve Araştırma Hastanesi), Ivana Nedic(St George's, University of London), Stéphanie Efthymiou(Queen Mary University of London), Hamid Galehdari(Shahid Chamran University of Ahvaz), Mohamad Tajik(Firoozgar General Hospital), Katharina Stumpfe(University Hospital Cologne), Farah Bibi(Pir Mehr Ali Shah Arid Agriculture University), Özkan Özdemir(Acıbadem University), Hüseyin Per(Erciyes University), Rosanne Sprute(University of Cologne), Ahmet Sami Güven(Necmettin Erbakan University), Bita Shalbafan(Tehran University of Medical Sciences), Yalda Jamshidi(St George's, University of London), Jawaher Zeighami, Neda Mazaheri(Shahid Chamran University of Ahvaz), Reza Azizi Malamiri(Ahvaz Jundishapur University of Medical Sciences), Henry Houlden(Queen Mary University of London), Emily Cooper(St George's, University of London), Ayşe Kaçar Bayram(Kayseri Eğitim ve Araştırma Hastanesi), Gholamreza Shariati(Ahvaz Jundishapur University of Medical Sciences), Tipu Sultan(Cukurova University), Vincenzo Salpietro(University College London), Nurettin Bayram(Kayseri Eğitim ve Araştırma Hastanesi), Matthias Pergande(University Hospital Cologne), Seyed Kianoosh Naghibzadeh(Islamic Azad University, Tehran)
Cited by 13
Related Papers
Genome-wide association study reveals genetic risk underlying Parkinson's disease
|Nature Genetics|2009|2k
Biallelic expansion of an intronic repeat in RFC1 is a common cause of late-onset ataxia
|Nature Genetics|2019|592
Global guideline for the diagnosis and management of rare mould infections: an initiative of the European Confederation of Medical Mycology in cooperation with the International Society for Human and Animal Mycology and the American Society for Microbiology
|The Lancet Infectious Diseases|2021|450
Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel
|Nature Communications|2015|387