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Metabolic consequences of a novel missense mutation of the mtDNA CO I gene.
Varlamov DA, Kudin AP, Vielhaber S, Schröder R, Sassen R, Becker A, Kunz D, Haug K, Rebstock J, Heils A, Elger CE, Kunz WS. Varlamov DA, et al. Among authors: kunz d, kunz ws. Hum Mol Genet. 2002 Aug 1;11(16):1797-805. doi: 10.1093/hmg/11.16.1797. Hum Mol Genet. 2002. PMID: 12140182
Mitochondrial dysfunction in myofibrillar myopathy.
Reimann J, Kunz WS, Vielhaber S, Kappes-Horn K, Schröder R. Reimann J, et al. Among authors: kunz ws. Neuropathol Appl Neurobiol. 2003 Feb;29(1):45-51. doi: 10.1046/j.1365-2990.2003.00428.x. Neuropathol Appl Neurobiol. 2003. PMID: 12581339
290 results