Genetics of Mitochondrial Disease with Focus on Movement Disorders
Author:
Publisher
Springer International Publishing
Link
http://link.springer.com/content/pdf/10.1007/978-3-319-17223-1_18
Reference93 articles.
1. Finsterer J. Inherited mitochondrial disorders. Adv Exp Med Biol. 2012;942:187–213.
2. Finsterer J. Central nervous system manifestations of mitochondrial disorders. Acta Neurol Scand. 2006;114:217–38.
3. Donaldson I, Marsden CD, Schneider S, Bhatia K. Marsden’s book of movement disorders. Oxford: Oxford University Press; 2012. ISBN 978-0-19-261911-2.
4. Gui YX, Xu ZP, Lv W, Liu HM, Zhao JJ, Hu XY. Association of mitochondrial DNA polymerase γ gene POLG1 polymorphisms with parkinsonism in Chinese populations. PLoS One. 2012;7(12):e50086. doi: 10.1371/journal.pone.0050086 .
5. Mukai M, Sugaya K, Yabe I, Goto Y, Yokochi F, Miyamoto K, Cai H, Sasaki H, Matsubara S. Neuromelanin MRI in a family with mitochondrial parkinsonism harboring a Y955C mutation in POLG1. Parkinsonism Relat Disord. 2013;19:821–4.
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