المؤلفون: B. Mousson de Camaret, Christophe Vial, Andoni Echaniz-Laguna, Stéphane Allouche, Patrizia Amati-Bonneau, Christine Tranchant, Lucie Guyant-Maréchal, Armelle Magot, M. Goideau-Sevrain, Mathieu Anheim, Thierry Kuntzer, A.-L. Bédat-Millet, Christophe Verny, N. Carvalho, C. Acquaviva-Bourdain, Philippe Petiot, Xavier Ayrignac, Guilhem Solé, Salah Omer, M. Béreau, M. Barth, Guillaume Taieb, François Ochsner, Stéphane Kremer, Grégory Tio

المساهمون: Biologie Neurovasculaire et Mitochondriale Intégrée (BNMI), Université d'Angers (UA)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)

المصدر: J Neurol Sci
J Neurol Sci, 2016, 368, pp.70-6. ⟨10.1016/j.jns.2016.06.062⟩

مصطلحات موضوعية: 0301 basic medicine, Adult, Male, Mitochondrial DNA, Encephalopathy, Mutation, Missense, Mitochondrial diseases, DNA-Directed DNA Polymerase, Biology, Ophthalmoparesis, Tertiary Care Centers, 03 medical and health sciences, Dysarthria, Young Adult, 0302 clinical medicine, Genotype, medicine, 80 and over, Missense mutation, Humans, Age of Onset, Genetic Association Studies, Aged, Retrospective Studies, Genetics, Aged, 80 and over, Cerebellar ataxia, Muscles, Brain, Middle Aged, medicine.disease, Magnetic Resonance Imaging, 3. Good health, DNA Polymerase gamma, Europe, 030104 developmental biology, Mitochondrial respiratory chain, Phenotype, Neurology, Mutation, Female, Neurology (clinical), medicine.symptom, Missense, 030217 neurology & neurosurgery, [SDV.MHEP]Life Sciences [q-bio]/Human health and pathology

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::860836ddbd99a481d1c882ef22b371b6
https://hal.archives-ouvertes.fr/hal-02066824

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