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Mitochondrial HMG–CoA Synthase Deficiency

By María Arnedo, Mónica Ramos, Beatriz Puisac, Ma Concepción Gil-Rodríguez, Esperanza Teresa, Ángeles Pié, Gloria Bueno, Feliciano J. Ramos, Paulino Gómez-Puertas and Juan Pie

Submitted: November 17th 2010Reviewed: July 2nd 2011Published: November 21st 2011

DOI: 10.5772/22151

Downloaded: 2305

© 2011 The Author(s). Licensee IntechOpen. This chapter is distributed under the terms of the Creative Commons Attribution 3.0 License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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María Arnedo, Mónica Ramos, Beatriz Puisac, Ma Concepción Gil-Rodríguez, Esperanza Teresa, Ángeles Pié, Gloria Bueno, Feliciano J. Ramos, Paulino Gómez-Puertas and Juan Pie (November 21st 2011). Mitochondrial HMG–CoA Synthase Deficiency, Advances in the Study of Genetic Disorders Kenji Ikehara, IntechOpen, DOI: 10.5772/22151. Available from:

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