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Merosin-deficient congenital muscular dystrophy. Partial genetic correction in two mouse models.
Humans and mice with deficiency of the alpha2 subunit of the basement membrane protein laminin-2/merosin suffer from merosin-deficient congenital muscular dystrophy (MCMD). We have expressed a human laminin alpha2 chain transgene under the regulation of a muscle-specific creatine kinase promoter in...
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| Gepubliceerd in: | J Clin Invest |
|---|---|
| Hoofdauteurs: | , , , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
American Society for Clinical Investigation
1998
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC508948/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/9710454/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI3705 |
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