Skip Nav Destination
Close Modal
Update search
Filter
- Title
- Author
- Author Affiliations
- Full Text
- Abstract
- Keyword
- DOI
- ISBN
- EISBN
- ISSN
- EISSN
- Issue
- Volume
- References
Filter
- Title
- Author
- Author Affiliations
- Full Text
- Abstract
- Keyword
- DOI
- ISBN
- EISBN
- ISSN
- EISSN
- Issue
- Volume
- References
Filter
- Title
- Author
- Author Affiliations
- Full Text
- Abstract
- Keyword
- DOI
- ISBN
- EISBN
- ISSN
- EISSN
- Issue
- Volume
- References
Filter
- Title
- Author
- Author Affiliations
- Full Text
- Abstract
- Keyword
- DOI
- ISBN
- EISBN
- ISSN
- EISSN
- Issue
- Volume
- References
Filter
- Title
- Author
- Author Affiliations
- Full Text
- Abstract
- Keyword
- DOI
- ISBN
- EISBN
- ISSN
- EISSN
- Issue
- Volume
- References
Filter
- Title
- Author
- Author Affiliations
- Full Text
- Abstract
- Keyword
- DOI
- ISBN
- EISBN
- ISSN
- EISSN
- Issue
- Volume
- References
NARROW
Format
Subjects
Journal
Article Type
TOC Section
Date
Availability
1-3 of 3
Keywords: Neuromuscular disorder
Close
Follow your search
Access your saved searches in your account
Would you like to receive an alert when new items match your search?
Sort by
Journal Articles
In collection:
Neuromuscular Disease
Suzie Buono, Arnaud Monseur, Alexia Menuet, Anne Robé, Catherine Koch, Jocelyn Laporte, Leen Thielemans, Marion Depla, Belinda S. Cowling
Journal:
Disease Models & Mechanisms
Dis Model Mech (2022) 15 (7): dmm049284.
Published: 25 July 2022
... oligonucleotide Therapy Neuromuscular disorder Dynacure Be Est Projets d'Avenir du programme d'Investissement Avenir 3 coDyn101 In a research setting, mouse models of disease provide an excellent tool to investigate disease pathophysiology and test therapeutic approaches. Mouse...
Includes: Supplementary data
Journal Articles
Johann Böhm, Inès Barthélémy, Charlène Landwerlin, Nicolas Blanchard-Gutton, Frédéric Relaix, Stéphane Blot, Jocelyn Laporte, Laurent Tiret
Journal:
Disease Models & Mechanisms
Dis Model Mech (2022) 15 (4): dmm049219.
Published: 14 April 2022
... DNM2 mutation associated with autosomal dominant centronuclear myopathy in humans. Neuromuscular disorder Congenital myopathy Dynamin Large animal model T-tubules MTM1 Fondation Maladies Rares 11734 Association Française contre les Myopathies http://dx.doi.org...
Includes: Supplementary data
Journal Articles
Journal:
Disease Models & Mechanisms
Dis Model Mech (2014) 7 (12): 1407–1415.
Published: 1 December 2014
... J. C. , Hamroun D. ( 2013 ). The 2014 version of the gene table of monogenic neuromuscular disorders (nuclear genome) . Neuromuscul. Disord. 23 , 1081 – 1111 . Laing N. G. , Wilton S. D. , Akkari P. A. , Dorosz S. , Boundy K. , Kneebone C...
Includes: Supplementary data