Diagnosis and Treatment of Mitochondrial Myopathies
Author:
Funder
Wellcome Trust
Medical Research Council
Publisher
Springer Science and Business Media LLC
Subject
Pharmacology (medical),Clinical Neurology,Pharmacology
Link
http://link.springer.com/article/10.1007/s13311-018-00674-4/fulltext.html
Reference78 articles.
1. Gorman GS, Chinnery PF, DiMauro S et al. Mitochondrial diseases. Nat Rev Dis Primers, 2, 16080 (2016).
2. Shoffner JM, Lott MT, Voljavec AS, Soueidan SA, Costigan DA, Wallace DC. Spontaneous Kearns-Sayre/chronic external ophthalmoplegia plus syndrome associated with a mitochondrial DNA deletion: a slip-replication model and metabolic therapy. Proc Natl Acad Sci U S A, 86(20), 7952–7956 (1989).
3. Rossignol R, Faustin B, Rocher C, Malgat M, Mazat JP, Letellier T. Mitochondrial threshold effects. Biochem J, 370(Pt 3), 751–762 (2003).
4. Smith AC, Robinson AJ. MitoMiner v3.1, an update on the mitochondrial proteomics database. Nucleic Acids Res, 44(D1), D1258–D1261 (2016).
5. Sommerville EW, Chinnery PF, Gorman GS, Taylor RW. Adult-onset Mendelian PEO Associated with Mitochondrial Disease. J Neuromuscul Dis, 1(2), 119–133 (2014).
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