Mitochondrial DNA variants in Bulgarian patients affected by multiple sclerosis
Author:
Publisher
Wiley
Subject
Neurology (clinical),Neurology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1468-1331.2006.01541.x/fullpdf
Reference22 articles.
1. Association of the 11778 mitochondria1 DNA mutation and demyelinating disease
2. OCCURRENCE OF A MULTIPLE SCLEROSIS-LIKE ILLNESS IN WOMEN WHO HAVE A LEBER'S HEREDITARY OPTIC NEUROPATHY MITOCHONDRIAL DNA MUTATION
3. Leber's hereditary optic neuropathy associated with a disorder indistinguishable from multiple sclerosis in a male harbouring the mitochondrial DNA 11778 mutation
4. Leber's Hereditary Optic Neuropathy Mitochondrial DNA Mutations in Childhood Multiple Sclerosis*
5. Mitochondrial DNA mutations in multiple sclerosis
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1. Mitochondrial DNA haplogroup analysis in Saudi Arab patients with multiple sclerosis;PLOS ONE;2022-12-19
2. Analysis of the entire mitochondrial genome reveals Leber’s hereditary optic neuropathy mitochondrial DNA mutations in an Arab cohort with multiple sclerosis;Scientific Reports;2022-06-30
3. Next-generation sequencing of the whole mitochondrial genome identifies functionally deleterious mutations in patients with multiple sclerosis;PLOS ONE;2022-02-07
4. Mitonuclear interactions influence multiple sclerosis risk;Gene;2020-10
5. The role of mitochondria in pathological mechanisms of innate immunity in multiple;Zhurnal nevrologii i psikhiatrii im. S.S. Korsakova;2020
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