Fatigue in primary genetic mitochondrial disease: No rest for the weary-Reference-Cited by-同舟云学术

Fatigue in primary genetic mitochondrial disease: No rest for the weary

Published:2019-11 Issue:11 Volume:29 Page:895-902
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Parikh Sumit,Galioto Rachel,Lapin Brittany,Haas Richard,Hirano Michio,Koenig Mary Kay,Saneto Russell P.^ORCID,Zolkipli-Cunningham Zarazuela,Goldstein Amy,Karaa Amel

Publisher

Elsevier BV

Subject

Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health

Reference57 articles.

1. De novo mtDNA point mutations are common and have a low recurrence risk;Sallevelt;J Med Genet,2017

2. The incidence of mitochondrial encephalomyopathies in childhood: clinical features and morphological, biochemical, and DNA abnormalities;Darin;Ann Neurol,2001

3. Incidence of primary mitochondrial disease in children younger than 2 years presenting with acute liver failure;McKiernan;J Pediatr Gastroenterol Nutr,2016

4. Mitochondrial disorders overview;Chinnery,1993

5. Prevalence of nuclear and mitochondrial DNA mutations related to adult mitochondrial disease;Gorman;Ann Neurol,2015

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