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Zebrafish Models of LAMA2-Related Congenital Muscular Dystrophy (MDC1A)
LAMA2-related congenital muscular dystrophy (CMD; LAMA2-MD), also referred to as merosin deficient CMD (MDC1A), is a severe neonatal onset muscle disease caused by recessive mutations in the LAMA2 gene. LAMA2 encodes laminin α2, a subunit of the extracellular matrix (ECM) oligomer laminin 211. There...
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| Vydáno v: | Front Mol Neurosci |
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| Hlavní autoři: | , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Frontiers Media S.A.
2020
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7364686/ https://ncbi.nlm.nih.gov/pubmed/32742259 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fnmol.2020.00122 |
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