LAMA2 Neuropathies: Human Findings and Pathomechanisms From Mouse Models

Merosin deficient Congenital Muscular Dystrophy (MDC1A), or LAMA2-related muscular dystrophy (LAMA2-RD), is a recessive disorder resulting from mutations in the LAMA2 gene, encoding for the alpha-2 chain of laminin-211. The disease is predominantly characterized by progressive muscular dystrophy aff...

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Detalles Bibliográficos
Autores principales: Previtali, Stefano Carlo, Zambon, Alberto Andrea
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7190814/
https://www.ncbi.nlm.nih.gov/pubmed/32390798
http://dx.doi.org/10.3389/fnmol.2020.00060

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7190814/
https://www.ncbi.nlm.nih.gov/pubmed/32390798
http://dx.doi.org/10.3389/fnmol.2020.00060

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