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المؤلفون: Theodora Markati, Maryam Oskoui, Michelle A Farrar, Tina Duong, Nathalie Goemans, Laurent Servais
المصدر: The Lancet Neurology. 21:814-829
مصطلحات موضوعية: Dystrophin, Muscular Dystrophy, Duchenne, Genotype, Humans, Exons, Genetic Therapy, Neurology (clinical)
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::820ad3542d282c18a7729900e4d102abTest
https://doi.org/10.1016/s1474-4422Test(22)00125-9 -
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المؤلفون: S. Dorricott, Sjef J. de Kimpe, J.C.T. van Deutekom, Alessandra Ferlini, R. Wilson, Mar Tulinius, Annarita Armaroli, Afrodite Lourbakos, Erik H. Niks, G. Campion, Nathalie Goemans, A. Morgan
المصدر: Neuromuscular Disorders. 23:847
مصطلحات موضوعية: musculoskeletal diseases, congenital, hereditary, and neonatal diseases and abnormalities, education.field_of_study, medicine.medical_specialty, biology, Duchenne muscular dystrophy, Population, Skeletal muscle, medicine.disease, Molecular biology, Exon skipping, Exon, Endocrinology, medicine.anatomical_structure, Neurology, Internal medicine, Pediatrics, Perinatology and Child Health, biology.protein, medicine, Neurology (clinical), Muscular dystrophy, Dystrophin, education, Genetics (clinical), Drisapersen
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::5f553433245233ec76deff1fccf241cfTest
https://doi.org/10.1016/j.nmd.2013.06.718Test