المؤلفون: C. Verny, N. Guegen, V. Desquiret-Dumas, A. Chevrollier, A. Prundean, F. Dubas, J. Cassereau, M. Ferré, P. Amati-Bonneau, D. Bonneau, P. Reynier, V. Procaccio

المصدر: Mitochondrion

مصطلحات موضوعية: Adult, DNA, Mitochondrial/analysis/genetics, Female, Genes, Mitochondrial, Humans, Male, Middle Aged, Mitochondria/enzymology/genetics, Mitochondrial Proton-Translocating ATPases/genetics/metabolism, Phenotype, Point Mutation, Spastic Paraplegia, Hereditary/genetics

العلاقة: http://okina.univ-angers.fr/publications/ua8265Test

الإتاحة: https://doi.org/10.1016/j.mito.2010.07.006Test
http://okina.univ-angers.fr/publications/ua8265Test

المؤلفون: Naig Guegen, Dominique Bonneau, Patrizia Amati-Bonneau, Frédéric Dubas, Julien Cassereau, Marc Ferré, Valérie Desquiret, Christophe Verny, Arnaud Chevrollier, Pascal Reynier, Vincent Procaccio, Adriana Prundean

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), Mitochondrie : Régulations et Pathologie, Université d'Angers (UA)-Institut National de la Santé et de la Recherche Médicale (INSERM), Biologie Neurovasculaire Intégrée (BNVI), Centre National de la Recherche Scientifique (CNRS)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Université d'Angers (UA)

المصدر: Mitochondrion
Mitochondrion, 2010, 11 (1), pp.70-75. ⟨10.1016/j.mito.2010.07.006⟩

مصطلحات موضوعية: Adult, Male, Mitochondrial DNA, Mitochondrial/analysis/genetics, Hereditary spastic paraplegia, Mitochondrial disease, [SDV]Life Sciences [q-bio], Mitochondrion, Biology, medicine.disease_cause, DNA, Mitochondrial, 03 medical and health sciences, 0302 clinical medicine, Mitochondria/enzymology/genetics, medicine, Spastic Paraplegia, Humans, Point Mutation, Molecular Biology, 030304 developmental biology, Genetics, 0303 health sciences, Mutation, Genetic heterogeneity, Spastic Paraplegia, Hereditary, Point mutation, Cell Biology, DNA, Middle Aged, Mitochondrial Proton-Translocating ATPases, medicine.disease, 3. Good health, nervous system diseases, Mitochondrial, Mitochondria, Genes, Mitochondrial, Phenotype, Genes, Molecular Medicine, Hereditary/genetics, Female, Mitochondrial Proton-Translocating ATPases/genetics/metabolism, 030217 neurology & neurosurgery, Human mitochondrial DNA haplogroup

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b67090e30a2fa85b4370ac8c732a452Test
https://pubmed.ncbi.nlm.nih.gov/20656066Test

المؤلفون: Verny, Christophe¹, Guegen, Naig^2,3, Desquiret, Valerie², Chevrollier, Arnaud^2,3, Prundean, Adriana¹, Dubas, Frederic¹, Cassereau, Julien^1,4, Ferre, Marc^2,3, Amati-Bonneau, Patrizia^2,3, Bonneau, Dominique^2,3, Reynier, Pascal^2,3, Procaccio, Vincent^2,4 ViProcaccio@chu-angers.fr

المصدر: Mitochondrion. Jan2011, Vol. 11 Issue 1, p70-75. 6p.

مصطلحات موضوعية: *PARAPLEGIA, *MITOCHONDRIAL pathology, *GENETIC mutation, *SYNDROMES, *BIOCHEMISTRY, *NECROSIS, *GENETICS