Phenotypic continuum of <scp><i>NFU1</i></scp>‐related disorders
Rauan Kaiyrzhanov(National Hospital for Neurology and Neurosurgery), Reza Maroofian(National Hospital for Neurology and Neurosurgery), Geneviève Bernard(McGill University Health Centre), Maria I. Scarano(Cooper University Health Care), Sambuddha Sen(The Ohio State University), J. A. Cowan(The Ohio State University), Christopher J. Carroll(St George's, University of London), Viorica Chelban(School of the Art Institute of Chicago), Shaimaa M. Khalaf(Assiut University), Maha S. Zaki(National Research Centre), Rachel Logan(Children's Healthcare of Atlanta), Kyle Thompson(Wellcome Centre for Mitochondrial Research), Mina Zamani(Shahid Chamran University of Ahvaz), Stéphanie Efthymiou(Queen Mary University of London), Hamid Galehdari(Shahid Chamran University of Ahvaz), Aizhan Zadagali(L. N. Gumilyov Eurasian National University), Mahmoud Y. Issa(National Research Centre), Houda Zghal Elloumi, Alireza Sedaghat(Ahvaz Jundishapur University of Medical Sciences), Yerdan Maidyrov(Kazakh National Medical University), Hasnaa M. Elbendary(National Human Genome Research Institute), Tracy Lau(National Hospital for Neurology and Neurosurgery), Ehsan Taghiabadi(Stem Cell Technology Research Center), Renkui Bai, Sumit Verma(Emory University), Jawaher Zeighami, Dinara Sadykova(Astana Medical University), Taru Hilander(University of Helsinki), Brian Kirmse(Jackson Memorial Hospital), Amanda Lindy(GenVec), Reza Azizi Malamiri(Ahvaz Jundishapur University of Medical Sciences), Andrés Moreno-De-Luca(Autism & Developmental Medicine Institute), Mohamed S. Abdel‐Hamid(National Research Centre), Henry Houlden(University College London), Kairgali Koneev(Kazakh National Medical University), Gözde Yeşil(Bezmiâlem Vakıf Üniversitesi), Gholamreza Shariati(Ahvaz Jundishapur University of Medical Sciences), Tahereh Seifi(Shahid Chamran University of Ahvaz), Katrina Allis, Robert W. Taylor(Wellcome Centre for Mitochondrial Research), Garry K. Brown(Churchill Hospital), Jaya Ganesh(Icahn School of Medicine at Mount Sinai), Richard Person(Baylor College of Medicine), Joseph J Gleeson(Howard Hughes Medical Institute), Ruth Brown(Churchill Hospital), Ismail Musab Gülaçar(Istanbul University)
Cited by 7
Related Papers
Clinical Whole-Exome Sequencing for the Diagnosis of Mendelian Disorders
|New England Journal of Medicine|2013|2k
Genome-wide association study reveals genetic risk underlying Parkinson's disease
|Nature Genetics|2009|2k