Genomic variants causing mitochondrial dysfunction are common in hereditary lower motor neuron disease-Reference-Cited by-同舟云学术

Genomic variants causing mitochondrial dysfunction are common in hereditary lower motor neuron disease

Published:2021-03-03 Issue:4 Volume:42 Page:460-472
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Human Mutation

Author:

Keller Natalie¹²³,Paketci Cem⁴,Altmueller Janine⁵,Fuhrmann Nico¹,Wunderlich Gilbert³⁶,Schrank Bertold⁷,Unver Olcay⁸,Yilmaz Sanem⁹,Boostani Reza¹⁰,Karimiani Ehsan Ghayoor¹¹,Motameny Susanne⁵,Thiele Holger⁵,Nürnberg Peter²⁵,Maroofian Reza¹¹,Yis Uluc⁴,Wirth Brunhilde¹²³^ORCID,Karakaya Mert¹²³^ORCID

Affiliation:

1. Institute of Human Genetics and Institute of Genetics University of Cologne Cologne Germany

2. Center for Molecular Medicine Cologne University of Cologne Cologne Germany

3. Center for Rare Diseases Cologne University Hospital Cologne Cologne Germany

4. Department of Pediatric Neurology Dokuz Eylül University Izmir Turkey

5. Cologne Center for Genomics (CCG) University of Cologne Cologne Germany

6. Department of Neurology University Hospital Cologne Cologne Germany

7. Department of Neurology DKD HELIOS Kliniken Wiesbaden Germany

8. Department of Pediatric Neurology Marmara University Istanbul Turkey

9. Department of Pediatric Neurology Ege University Izmir Turkey

10. Department of Neurology, Ghaem Hospital, Medical School Mashhad University of Medical Sciences Mashhad Iran

11. Molecular and Clinical Sciences Institute St. George's University of London, Cranmer Terrace London UK