Author:
Bertini Enrico,Rahman Shamima
Publisher
Springer International Publishing
Reference86 articles.
1. Bargiela D, Shanmugarajah P, Lo C, Blakely EL, Taylor RW, Horvath R, et al. Mitochondrial pathology in progressive cerebellar ataxia. Cerebellum Ataxias. 2015;2:16.
2. Pitceathly RD, Rahman S, Hanna MG. Single deletions in mitochondrial DNA – molecular mechanisms and disease phenotypes in clinical practice. Neuromuscul Disord. 2012;22(7):577–86.
3. Aure K, Ogier de Baulny H, Laforet P, Jardel C, Eymard B, Lombes A. Chronic progressive ophthalmoplegia with large-scale mtDNA rearrangement: can we predict progression? Brain. 2007;130(Pt 6):1516–24.
4. Thorburn DR, Rahman J, Rahman S. Mitochondrial DNA-associated leigh syndrome and NARP. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, LJH B, Stephens K, et al., editors. GeneReviews((R)). Seattle, WA: University of Washington, Seattle; 1993. University of Washington, Seattle. GeneReviews is a registered trademark of the University of Washington, Seattle. All rights reserved.
5. Mancuso M, Orsucci D, Angelini C, Bertini E, Carelli V, Comi GP, et al. Phenotypic heterogeneity of the 8344A>G mtDNA “MERRF” mutation. Neurology. 2013;80(22):2049–54.
Cited by
1 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献