Identifying trajectories of fatigue in patients with primary mitochondrial disease due to the m.3243A

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Identifying trajectories of fatigue in patients with primary mitochondrial disease due to the m.3243A > G variant

Published:2022-08-24 Issue:6 Volume:45 Page:1130-1142
ISSN:0141-8955
Container-title:Journal of Inherited Metabolic Disease
language:en
Short-container-title:J of Inher Metab Disea

Author:

Klein Inge‐Lot¹^ORCID,Verhaak Christianne M.¹,Smeitink Jan A. M.²,de Laat Paul³,Janssen Mirian C. H.⁴,Custers José A. E.¹

Affiliation:

1. Department of Medical Psychology Radboud University Medical Center, Radboud Institute for Health Sciences, Radboud Center for Mitochondrial Medicine Nijmegen The Netherlands

2. Department of Pediatrics Radboud university medical center, Radboud Institute for Molecular Life Sciences, Radboud Center for Mitochondrial Medicine Nijmegen The Netherlands

3. Department of Pediatrics Franciscus Gasthuis & Vlietland Rotterdam The Netherlands

4. Department of Internal Medicine Radboud university medical center, Radboud Institute for Molecular Life Sciences, Radboud Center for Mitochondrial Medicine Nijmegen The Netherlands

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jimd.12546

Reference63 articles.

1. International Workshop:

2. The genetics and pathology of oxidative phosphorylation

3. Mitochondrial disease in adults: recent advances and future promise

4. MELAS syndrome: Clinical manifestations, pathogenesis, and treatment options

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