Identification of mutations in the<i>MYO9A</i>gene in patients with congenital myasthenic syndrome
Congenital myasthenic syndromes are a group of rare and genetically heterogenous disorders resulting from defects in the structure and function of the neuromuscular junction. Patients with congenital myasthenic syndrome exhibit fatigable muscle weakness with a variety of accompanying phenotypes depe...
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| Main Authors: | , , , , , , , , , , , |
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| 格式: | Artigo |
| 語言: | 英语 |
| 出版: |
2016
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| 在線閱讀: | https://doi.org/10.1093/brain/aww130 |
| 標簽: |
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