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Prenatal muscle development in a mouse model for the secondary dystroglycanopathies
BACKGROUND: The defective glycosylation of α-dystroglycan is associated with a group of muscular dystrophies that are collectively referred to as the secondary dystroglycanopathies. Mutations in the gene encoding fukutin-related protein (FKRP) are one of the most common causes of secondary dystrogly...
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| Pubblicato in: | Skelet Muscle |
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| Autori principali: | , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
BioMed Central
2016
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4759920/ https://ncbi.nlm.nih.gov/pubmed/26900448 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13395-016-0073-y |
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