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Bridging integrator 1 (Bin1) deficiency in zebrafish results in centronuclear myopathy
Autosomal recessive centronuclear myopathy (CNM2), caused by mutations in bridging integrator 1 (BIN1), is a mildly progressive neuromuscular disorder characterized by abnormally centralized myonuclei and muscle weakness. BIN1 is important for membrane sensing and remodeling in vitro in different ce...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4049309/ https://ncbi.nlm.nih.gov/pubmed/24549043 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddu067 |
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