Motor neuron diseases caused by a novel VRK1 variant – A genotype/phenotype study

Author:

Sedghi Maryam1,Moslemi Ali‐Reza2,Olive Montse34,Etemadifar Masoud5,Ansari Behnaz6,Nasiri Jafar7,Emrahi Leila2,Mianesaz Hamid‐Reza8,Laing Nigel G.9,Tajsharghi Homa910ORCID

Affiliation:

1. Medical Genetics Laboratory Alzahra University HospitalIsfahan University of Medical Sciences Isfahan Iran

2. Department of Pathology University of GothenburgSahlgrenska University Hospital Gothenburg Sweden

3. Institute of NeuropathologyDepartment of PathologyInstitut Investigació Biomèdica de Bellvitge (IDIBELL)‐Hospital de Bellvitge Hospitalet de Llobregat08907Barcelona Spain

4. Neuromuscular Unit Department of Neurology Institut Investigació Biomèdica de Bellvitge‐(IDIBELL)‐Hospital de Bellvitge Hospitalet de Llobregat08907Barcelona Spain

5. Department of Functional Neursurgery Faculty of MedicineIsfahan University of Medical Sciences Isfahan Iran

6. Department of Neurology Faculty of Medicine Isfahan University of Medical Sciences Isfahan Iran

7. Department of Pediatric Neurology Faculty of Medicine Isfahan University of Medical Sciences Isfahan Iran

8. Department of Genetics and Molecular Biology Isfahan University of Medical Sciences Isfahan Iran

9. Centre for Medical Research The University of Western Australia and the Harry Perkins Institute for Medical Research Nedlands Western Australia Australia

10. School of Health Sciences Division Biomedicine and Translational Medicine University of Skovde Skovde Sweden

Funder

Vetenskapsrådet

Publisher

Wiley

Subject

Clinical Neurology,General Neuroscience

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