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Mechanisms of Disease: congenital muscular dystrophies—glycosylation takes center stage
Recent studies have defined a group of muscular dystrophies, now termed the dystroglycanopathies, as novel disorders of glycosylation. These conditions include Walker–Warburg syndrome, muscle–eye–brain disease, Fukuyama-type congenital muscular dystrophy, congenital muscular dystrophy types 1C and 1...
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
2006
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| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2855642/ https://ncbi.nlm.nih.gov/pubmed/16932553 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ncpneuro0155 |
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