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Congenital myasthenia–related AChR δ subunit mutation interferes with intersubunit communication essential for channel gating
Congenital myasthenias (CMs) arise from defects in neuromuscular junction–associated proteins. Deciphering the molecular bases of the CMs is required for therapy and illuminates structure-function relationships in these proteins. Here, we analyze the effects of a mutation in 1 of 4 homologous subuni...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
American Society for Clinical Investigation
2008
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2289798/ https://ncbi.nlm.nih.gov/pubmed/18398509 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI34527 |
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