-
1
المؤلفون: Eva Trevisson, Karine Auré, Anne Lombès, Gabriele Siciliano, Sabrina Sacconi, Odile Rigal, Corrado Angelini, Paola Tonin, Leonardo Salviati, Ségolène Aymé, Alberto Garcia Redondo, Claude Desnuelle, Michelangelo Mancuso
المساهمون: Institut de signalisation, biologie du développement et cancer (ISBDC), Centre National de la Recherche Scientifique (CNRS)-Université Nice Sophia Antipolis (... - 2019) (UNS), COMUE Université Côte d'Azur (2015-2019) (COMUE UCA)-COMUE Université Côte d'Azur (2015-2019) (COMUE UCA)-Université Côte d'Azur (UCA), CHU Nice, Université Nice Sophia Antipolis (... - 2019) (UNS), COMUE Université Côte d'Azur (2015-2019) (COMUE UCA)-COMUE Université Côte d'Azur (2015-2019) (COMUE UCA), Dpt. of Pediatrics, Universita degli Studi di Padova, Cartographie du Genome Humain a des Fins de Recherche Clinique, Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut National de la Santé et de la Recherche Médicale (INSERM), Service de Biochimie, Hôpital Robert Debré, Physiopathologie et thérapie du muscle strié, Université Pierre et Marie Curie - Paris 6 (UPMC)-IFR14-Institut National de la Santé et de la Recherche Médicale (INSERM), COMUE Université Côte d'Azur (2015-2019) (COMUE UCA), Université Nice Sophia Antipolis (1965 - 2019) (UNS), COMUE Université Côte d'Azur (2015-2019) (COMUE UCA)-COMUE Université Côte d'Azur (2015-2019) (COMUE UCA)-Centre National de la Recherche Scientifique (CNRS)-Université Côte d'Azur (UCA), Università degli Studi di Padova = University of Padua (Unipd)
المصدر: Neuromuscul Disord
Neuromuscul Disord, 2010, 20 (1), pp.44-8. ⟨10.1016/j.nmd.2009.10.014⟩مصطلحات موضوعية: Male, Ubiquinone, Myopathy, medicine.disease_cause, Bioinformatics, Cohort Studies, chemistry.chemical_compound, 0302 clinical medicine, Mitochondrial myopathy, Child, [SDV.BDD]Life Sciences [q-bio]/Development Biology, Genetics (clinical), Chromatography, High Pressure Liquid, Genetics, Aged, 80 and over, 0303 health sciences, Mutation, food and beverages, Mitochondrial Myopathies, Middle Aged, Phenotype, Treatment Outcome, Neurology, Child, Preschool, Female, medicine.symptom, Coenzyme Q10 deficiency, Adult, Mitochondrial DNA, Adolescent, Mitochondrial disease, Coenzyme Q10, Treatment, Biology, DNA, Mitochondrial, 03 medical and health sciences, Young Adult, medicine, Humans, Muscle, Skeletal, 030304 developmental biology, Aged, medicine.disease, chemistry, Coenzyme Q – cytochrome c reductase, Pediatrics, Perinatology and Child Health, Neurology (clinical), 030217 neurology & neurosurgery
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa1512d6fae66b55769ff69c67f0055fTest
https://pubmed.ncbi.nlm.nih.gov/19945282Test -
2
المؤلفون: Douglass M. Turnbull, A. Saunières, B. Mousson de Camaret, Véronique Paquis-Flucklinger, B. Vialettes, Claude Desnuelle, H. Narbonne, D. Perucca-Lostanlen, Robert W. Taylor, C Hayes
المصدر: Biochimica et biophysica acta. 1588(3)
مصطلحات موضوعية: Mitochondrial DNA, Genotype, Mutant, Respiratory chain, Biology, Mitochondrion, Deafness, DNA, Mitochondrial, Cell Fusion, Diabetes Complications, 03 medical and health sciences, Diabetes mellitus genetics, Electron Transport Complex III, 0302 clinical medicine, Multienzyme Complexes, Diabetes Mellitus, Humans, Point Mutation, NADH, NADPH Oxidoreductases, Mitochondrial diabetes, Molecular Biology, Transmitochondrial cybrid, 030304 developmental biology, Genetics, 0303 health sciences, Homoplasmy, Electron Transport Complex I, Base Sequence, Point mutation, Electron Transport Complex II, Fibroblasts, Blotting, Northern, Molecular biology, Heteroplasmy, RNA, Transfer, Glu, Clone Cells, Succinate Dehydrogenase, Molecular Medicine, Oxidoreductases, 030217 neurology & neurosurgery
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93d57488e5e143ad1c6b4ea6a8969579Test
https://pubmed.ncbi.nlm.nih.gov/12393175Test