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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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| 出版年: | Skelet Muscle |
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| 主要な著者: | , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
BioMed Central
2016
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| 主題: | |
| オンライン･アクセス: | 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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