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Showing results (251-260 of 254) with videos related to

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Neurology|June 8, 2011
RRM2B mutations are frequent in familial PEO with multiple mtDNA deletionsC Fratter, P Raman, C L Alston, et al.
Journal of Medical Genetics|March 3, 2009
Novel POLG1 mutations associated with neuromuscular and liver phenotypes in adults and childrenJ D Stewart, S Tennant, H Powell, et al.
Neurology|May 19, 2010
The clinical, histochemical, and molecular spectrum of PEO1 (Twinkle)-linked adPEOC Fratter, G S Gorman, J D Stewart, et al.
Brain : a Journal of Neurology|February 17, 2010
Multi-system neurological disease is common in patients with OPA1 mutationsP Yu-Wai-Man, P G Griffiths, G S Gorman, et al.
Pageof 26

Showing results (251-260 of 254) with videos related to

Sort By:
Pageof 26
You have reached the last page of results.This site can display upto 254 results.
Neurology|June 8, 2011
RRM2B mutations are frequent in familial PEO with multiple mtDNA deletionsC Fratter, P Raman, C L Alston, et al.
Journal of Medical Genetics|March 3, 2009
Novel POLG1 mutations associated with neuromuscular and liver phenotypes in adults and childrenJ D Stewart, S Tennant, H Powell, et al.
Neurology|May 19, 2010
The clinical, histochemical, and molecular spectrum of PEO1 (Twinkle)-linked adPEOC Fratter, G S Gorman, J D Stewart, et al.
Brain : a Journal of Neurology|February 17, 2010
Multi-system neurological disease is common in patients with OPA1 mutationsP Yu-Wai-Man, P G Griffiths, G S Gorman, et al.
Pageof 26