المؤلفون: Colleen M. Donlin-Smith, Sabrina Sacconi, Rabi Tawil, Jeffrey Statland, Constantine Farmakidis, Mina Chung

المساهمون: Institut de Biologie Valrose (IBV), Université Nice Sophia Antipolis (... - 2019) (UNS), COMUE Université Côte d'Azur (2015-2019) (COMUE UCA)-COMUE Université Côte d'Azur (2015-2019) (COMUE UCA)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Université Côte d'Azur (UCA)

المصدر: Neurology
Neurology, American Academy of Neurology, 2013, 80 (13), pp.1247-50. ⟨10.1212/WNL.0b013e3182897116⟩

مصطلحات موضوعية: Adult, Male, musculoskeletal diseases, congenital, hereditary, and neonatal diseases and abnormalities, medicine.medical_specialty, Biology, Article, Muscular Dystrophies, Fragment size, 03 medical and health sciences, 0302 clinical medicine, Interquartile range, Internal medicine, medicine, Humans, Facioscapulohumeral muscular dystrophy, Registries, Coats' disease, Muscular dystrophy, [SDV.BDD]Life Sciences [q-bio]/Development Biology, Dystrophy, Middle Aged, medicine.disease, Muscular Dystrophy, Facioscapulohumeral, Confidence interval, Surgery, Tandem Repeat Sequences, Mutation, 030221 ophthalmology & optometry, Retinal Telangiectasis, Female, Neurology (clinical), Chromosomes, Human, Pair 4, Complication, 030217 neurology & neurosurgery, Muscle Contraction

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83487b42427add4b4a98623657c6dd64
https://doi.org/10.1212/wnl.0b013e3182897116