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Mitochondrial complex I activity is significantly decreased in a patient with maternally inherited type 2 diabetes mellitus and hypertrophic cardiomyopathy associated with mitochondrial DNA C3310T mutation: a cybrid study.
Chen J, Hattori Y, Nakajima K, Eizawa T, Ehara T, Koyama M, Hirai T, Fukuda Y, Kinoshita M, Sugiyama A, Hayashi J, Onaya T, Kobayashi T, Tawata M. Chen J, et al. Among authors: onaya t. Diabetes Res Clin Pract. 2006 Nov;74(2):148-53. doi: 10.1016/j.diabres.2006.03.024. Epub 2006 Jul 10. Diabetes Res Clin Pract. 2006. PMID: 16828917
Screening for genetic mutations. A review.
Tawata M, Aida K, Onaya T. Tawata M, et al. Among authors: onaya t. Comb Chem High Throughput Screen. 2000 Feb;3(1):1-9. doi: 10.2174/1386207003327756. Comb Chem High Throughput Screen. 2000. PMID: 10702609 Review.
243 results