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Journal of Neurology, Neurosurgery, and Psychiatry
|
July 20, 2004
No association of the mitochondrial DNA A12308G polymorphism with increased risk of stroke in patients with the A3243G mutation
M Deschauer, P F Chinnery, A M Schaefer, et al.
Neurology
|
April 28, 2004
Catastrophic presentation of mitochondrial disease due to a mutation in the tRNA(His) gene
R W Taylor, A M Schaefer, M T McDonnell, et al.
Neurology
|
August 29, 2007
Homoplasmy, heteroplasmy, and mitochondrial dystonia
R McFarland, P F Chinnery, E L Blakely, et al.
Neurology
|
June 8, 2011
RRM2B mutations are frequent in familial PEO with multiple mtDNA deletions
C Fratter, P Raman, C L Alston, et al.
Page
of 3
Search research articles
Search
Showing results (21-30 of 24) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 24 results.
Journal of Neurology, Neurosurgery, and Psychiatry
|
July 20, 2004
No association of the mitochondrial DNA A12308G polymorphism with increased risk of stroke in patients with the A3243G mutation
M Deschauer, P F Chinnery, A M Schaefer, et al.
Neurology
|
April 28, 2004
Catastrophic presentation of mitochondrial disease due to a mutation in the tRNA(His) gene
R W Taylor, A M Schaefer, M T McDonnell, et al.
Neurology
|
August 29, 2007
Homoplasmy, heteroplasmy, and mitochondrial dystonia
R McFarland, P F Chinnery, E L Blakely, et al.
Neurology
|
June 8, 2011
RRM2B mutations are frequent in familial PEO with multiple mtDNA deletions
C Fratter, P Raman, C L Alston, et al.
Page
of 3