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	21.	Human CIA30 is involved in the early assembly of mitochondrial complex I and mutations in its gene cause disease. [electronic resource] by Dunning, C J R McKenzie, M Sugiana, C Lazarou, M Silke, J Connelly, A Fletcher, J M Kirby, D M Thorburn, D R Ryan, M T Producer: 20071127 In: The EMBO journal vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	22.	Transmitochondrial embryonic stem cells containing pathogenic mtDNA mutations are compromised in neuronal differentiation. [electronic resource] by Kirby, D M Rennie, K J Smulders-Srinivasan, T K Acin-Perez, R Whittington, M Enriquez, J-A Trevelyan, A J Turnbull, D M Lightowlers, R N Producer: 20090803 In: Cell proliferation vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	23.	The mitochondrial DNA C3303T mutation can cause cardiomyopathy and/or skeletal myopathy. [electronic resource] by Bruno, C Kirby, D M Koga, Y Garavaglia, B Duran, G Santorelli, F M Shield, L K Xia, W Shanske, S Goldstein, J D Iwanaga, R Akita, Y Carrara, F Davis, A Zeviani, M Thorburn, D R DiMauro, S Producer: 19990824 In: The Journal of pediatrics vol. 135 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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