Myotubular myopathy and the neuromuscular junction: a novel therapeutic approach from mouse models
Author:
Affiliation:
1. University of Michigan, MI, USA;
2. Généthon, Evry, France;
3. Nationwide Children's Hospital, OH, USA;
4. IGBMC, Illkirch, France;
5. Children's Hospital Boston, MA, USA
Abstract
Publisher
The Company of Biologists
Subject
General Biochemistry, Genetics and Molecular Biology,Immunology and Microbiology (miscellaneous),Medicine (miscellaneous),Neuroscience (miscellaneous)
Link
http://journals.biologists.com/dmm/article-pdf/5/6/852/1865709/852.pdf
Reference44 articles.
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2. Lack of desmin results in abortive muscle regeneration and modifications in synaptic structure;Agbulut;Cell Motil. Cytoskeleton,2001
3. T-tubule biogenesis and triad formation in skeletal muscle and implication in human diseases;Al-Qusairi;Skelet. Muscle,2011
4. T-tubule disorganization and defective excitation-contraction coupling in muscle fibers lacking myotubularin lipid phosphatase;Al-Qusairi;Proc. Natl. Acad. Sci. USA,2009
5. X-linked recessive myotubular myopathy: II. Muscle morphology and human myogenesis;Ambler;Hum. Pathol.,1984
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