Author:
Garrido-Maraver Juan,Paz Marina Villanueva,Cordero Mario D.,Bautista-Lorite Juan,Oropesa-Ávila Manuel,de la Mata Mario,Pavón Ana Delgado,de Lavera Isabel,Alcocer-Gómez Elizabet,Galán Fernando,Ybot González Patricia,Cotán David,Jackson Sandra,Sánchez-Alcázar José A.
Funder
Ministerio de Sanidad, Spain
Fondo Europeo de Desarrollo Regional (FEDER-Unión Europea)
Proyecto de Investigación de Excelencia de la Junta de Andalucía
AEPMI (Asociación de Enfermos de Patología Mitocondrial)
Subject
Molecular Biology,Molecular Medicine
Reference84 articles.
1. Mitochondriopathies;Finsterer;Eur. J. Neurol.,2004
2. MELAS syndrome: characteristic migrainous and epileptic features and maternal transmission;Montagna;Neurology,1988
3. Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: a distinctive clinical syndrome;Pavlakis;Ann. Neurol.,1984
4. Mitochondrial encephalopathy, lactic acidosis, and strokelike episodes: basic concepts, clinical phenotype, and therapeutic management of MELAS syndrome;Sproule;Ann. N. Y. Acad. Sci.,2008
5. The mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episode syndrome-associated human mitochondrial tRNALeu(UUR) mutation causes aminoacylation deficiency and concomitant reduced association of mRNA with ribosomes;Chomyn;J. Biol. Chem.,2000
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