Valérie Biancalana

Publication Activity (10 Years)

Years Active: 2018-2021
Publications (10 Years): 2

Top Topics

Duchenne Muscular Dystrophy

Top Venues

Acta neuropathologica communications

This page only lists publications with an associated author ORCID identifier.

Publications

Xavière Lornage, Martial Mallaret, Roberto Silva-Rojas, Valérie Biancalana, Diane Giovannini, Klaus Dieterich, Safaa Saker, Jean François Deleuze, Bernard Wuyam, Jocelyn Laporte, Johann Böhm
Selective loss of a LAP1 isoform causes a muscle-specific nuclear envelopathy. Neurogenetics 22 (1) (2021)
Valérie Biancalana, Norma B Romero, Inger Johanne Thuestad, Jaakko Ignatius, Janne Kataja, Maria Gardberg, Delphine Héron, Edoardo Malfatti, Anders Oldfors, Jocelyn Laporte
Some DNM2 mutations cause extremely severe congenital myopathy and phenocopy myotubular myopathy. Acta neuropathologica communications 6 (1) (2018)