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Topic:   Mutation screen in genes of Complex I

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posted 11-27-2002 09:08 PM          Dear Colleagues: We developed methods to detect mutations in some nuclear DNA encoded subunits of Complex I for patients with metabolic encephalopathy / Leigh's like syndrome and Complex I deficiency, after the possibility of mutations in mitochondrial genes have been excluded. For patients who do not have access for mitochondrial DNA work up, we also can offer a comprehensive mitochondrial DNA analysis. ------------------ Bernadette Kalman, MD, PhD, Director of MS Research, Neurology, SLRHC, Columbia University, New York, NY 212-523-8676 [This message has been edited by Bernadette Kalman, MD,PhD (edited 11-27-2002).] IP: 141.155.63.6

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