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المؤلفون: Hans H. Jung, Michael Sinnreich, Jens A. Petersen, Wolfram Kress, Thierry Kuntzer, Angela Huebner, Elisabeth J. Rushing, Maja von der Hagen, Johannes Alexander Lobrinus, Veronika Kana, Dirk Fischer
المساهمون: University of Zurich, Petersen, Jens A
المصدر: BMC Neurology, Vol. 15 (2015) P. 182
BMC neurology
BMC Neurology
Bmc Neurology, vol. 15, no. 1, pp. 182مصطلحات موضوعية: Adult, Male, Heterozygote, Dysferlinopathy, Adolescent, Clinical Neurology, 10208 Institute of Neuropathology, Muscle Proteins, 610 Medicine & health, ddc:616.07, medicine.disease_cause, Dysferlin, Young Adult, medicine, Humans, Myopathy, ddc:611, Genetics, Mutation, biology, Genetic heterogeneity, business.industry, Homozygote, Haplotype, Membrane Proteins, General Medicine, Anatomy, Middle Aged, medicine.disease, Founder Effect, 10040 Clinic for Neurology, 3. Good health, 2728 Neurology (clinical), Phenotype, Muscular Dystrophies, Limb-Girdle, Female, Membrane Proteins/genetics, Muscle Proteins/genetics, Muscular Dystrophies, Limb-Girdle/genetics, Switzerland, biology.protein, Neurology (clinical), medicine.symptom, business, Research Article, Limb-girdle muscular dystrophy, Founder effect
وصف الملف: s12883-015-0449-3.pdf - application/pdf; application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b5d47ec334c3e9a41a950925d0c5859Test
https://doi.org/10.1186/s12883-015-0449-3Test -
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المؤلفون: Jacques S. Beckmann, Melissa J. Spencer
المصدر: Neuromuscular Disorders, vol. 18, no. 12, pp. 913-921
مصطلحات موضوعية: Sarcomeres, Gene isoform, Muscle Proteins, Models, Biological, Sarcomere, Article, medicine, Animals, Humans, Calpain/genetics, Calpain/metabolism, Muscle Proteins/genetics, Muscle Proteins/metabolism, Muscular Dystrophies, Limb-Girdle/genetics, Muscular Dystrophies, Limb-Girdle/metabolism, Mutation, Sarcomeres/metabolism, Muscular dystrophy, Genetics (clinical), Loss function, Genetics, biology, Calpain, Dystrophy, medicine.disease, Cell biology, Muscular Dystrophies, Limb-Girdle, Neurology, Pediatrics, Perinatology and Child Health, biology.protein, Titin, Neurology (clinical), Limb-girdle muscular dystrophy
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d38571d4127b7b2f9c161021bded730Test
https://doi.org/10.1016/j.nmd.2008.08.005Test -
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المؤلفون: A Meulemans, Sara Seneca, Linda De Meirleir, Joél Smet, Willy Lissens, Jan De Bleecker, Rudy Van Coster, Boel De Paepe
المساهمون: Faculty of Medicine and Pharmacy, Department of Embryology and Genetics, Pediatrics
المصدر: Vrije Universiteit Brussel
مصطلحات موضوعية: Muscle tissue, Mitochondrial DNA, Muscle Fibers, Skeletal, oxidative phosphorylation, Biology, DNA, Mitochondrial, law.invention, Restriction fragment, DNA, Mitochondrial/genetics, Electron Transport Complex IV, RNA, Transfer, Arts and Humanities (miscellaneous), law, Electron Transport Complex IV/genetics, medicine, Cytochrome c oxidase, oxidative phosphorylation system, Humans, Muscle, Skeletal, Myopathy, Muscle Fibers, Skeletal/pathology, Gene, Polymerase chain reaction, Mutation/physiology, Polymorphism, Single-Stranded Conformational, Genetics, mt disorders, Muscular Dystrophies, Limb-Girdle/genetics, Middle Aged, Molecular biology, Immunohistochemistry, Heteroplasmy, Blotting, Southern, medicine.anatomical_structure, Muscular Dystrophies, Limb-Girdle, Muscle, Skeletal/pathology, Mutation, biology.protein, Electrophoresis, Polyacrylamide Gel, Female, Neurology (clinical), medicine.symptom, DNA mutations, RNA, Transfer/genetics
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3537da1e5c6bb49f9ddfe86691abbba9Test
https://doi.org/10.1001/archneur.64.9.1339Test