Genetic basis of mitochondrial diseases
Author:
Affiliation:
1. Institute of Neurogenomics Helmholtz Zentrum München Neuherberg Germany
2. Institute of Human Genetics Technical University of Munich Germany
3. DZHK (German Centre for Cardiovascular Research) Partner Site Munich Heart Alliance Germany
Funder
Bundesministerium für Bildung und Forschung
Publisher
Wiley
Subject
Cell Biology,Genetics,Molecular Biology,Biochemistry,Structural Biology,Biophysics
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/1873-3468.14068
Reference273 articles.
1. Mitochondrial diseases
2. Lifetime risk of autosomal recessive mitochondrial disorders calculated from genetic databases
3. Clinical spectrum and diagnosis of mitochondrial disorders
4. NAD(P)HX dehydratase (NAXD) deficiency: a novel neurodegenerative disorder exacerbated by febrile illnesses
5. Therapies for mitochondrial diseases and current clinical trials
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