Genetic aetiology of ophthalmological manifestations in children - a focus on mitochondrial disease-related symptoms

Author:

Widgren Paula1234,Hurme Anri124,Falck Aura34,Keski-Filppula Riikka145,Remes Anne M67,Moilanen Jukka145,Majamaa Kari489,Kervinen Marko34,Uusimaa Johanna124

Affiliation:

1. PEDEGO Research Unit; University of Oulu; Oulu Finland

2. Department of Children and Adolescents; Division of Pediatric Neurology; Oulu University Hospital; Oulu Finland

3. Department of Ophthalmology; Oulu University Hospital; Oulu Finland

4. Medical Research Center Oulu; University of Oulu; Oulu Finland

5. Department of Clinical Genetics; Oulu University Hospital; Oulu Finland

6. Institute of Clinical Medicine - Neurology; University of Eastern Finland; Kuopio Finland

7. Department of Neurology; Kuopio University Hospital; Kuopio Finland

8. Research Unit of Clinical Neuroscience and Medical Research Center Oulu; University of Oulu; Oulu Finland

9. Department of Neurology; Oulu University Hospital; Oulu Finland

Funder

Suomen Lääketieteen Säätiö

Arvo and Lea Ylppo Foundation

Lastentautien Tutkimussäätiö

Evald and Hilda Nissi Foundation

Eye Foundation

Oulu University Hospital

Publisher

Wiley

Subject

Ophthalmology,General Medicine

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