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Neuromuscular Disorders : NMD|March 3, 2009
ETFDH mutations, CoQ10 levels, and respiratory chain activities in patients with riboflavin-responsive multiple acyl-CoA dehydrogenase deficiencyWen-Chen Liang, Aya Ohkuma, Yukiko K Hayashi, et al.Muscle & Nerve|February 12, 2009
Clinical and genetic analysis of lipid storage myopathiesAya Ohkuma, Satoru Noguchi, Hideo Sugie, et al.American Journal of Human Genetics|June 14, 2011
A congenital muscular dystrophy with mitochondrial structural abnormalities caused by defective de novo phosphatidylcholine biosynthesisSatomi Mitsuhashi, Aya Ohkuma, Beril Talim, et al.Pageof 2