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| Correction of pseudoexon splicing caused by a novel intronic dysferlin mutation JA Dominov, Ö Uyan, D McKenna‐Yasek, BRR Nallamilli, V Kergourlay, ... Annals of Clinical and Translational Neurology 6 (4), 642-654, 2019 | 21 | 2019 |
| Novel pathogenic variants in a French cohort widen the mutational spectrum of GNE myopathy M Cerino, S Gorokhova, A Béhin, JA Urtizberea, V Kergourlay, E Salvo, ... Journal of Neuromuscular Diseases 2 (2), 131-136, 2015 | 12 | 2015 |
| The dysferlin transcript containing the alternative exon 40a is essential for myocyte functions O Ballouhey, S Courrier, V Kergourlay, S Gorokhova, M Cerino, M Krahn, ... Frontiers in Cell and Developmental Biology 9, 754555, 2021 | 5 | 2021 |
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| TP 27 Characterization of the modular domains of dysferlin for gene transfer F Barthélémy, V Kergourlay, N Lévy, M Krahn, M Bartoli Neuromuscular Disorders 22 (9), 860-861, 2012 | 1 | 2012 |
| Let us know how access to this document benefits you. JA Dominov, O Uyan, D McKenna-Yasek, B Nallamilli, V Kergourlay, ... Neurology 6 (4), 642-654, 2019 | | 2019 |
| Mise au point d'outils novateurs pour l'identification de mutations pathogènes: le cas des dysferlinopathies V Kergourlay Aix-Marseille, 2014 | | 2014 |
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