Next-Generation Sequencing Identifies Transportin 3 as the Causative Gene for LGMD1F
Limb-girdle muscular dystrophies (LGMD) are genetically and clinically heterogeneous conditions. We investigated a large family with autosomal dominant transmission pattern, previously classified as LGMD1F and mapped to chromosome 7q32. Affected members are characterized by muscle weakness affecting...
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| Main Authors: | , , , , , , , , , , , , , |
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| 格式: | Artigo |
| 语言: | 英语 |
| 出版: |
2013
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| 在线阅读: | https://doi.org/10.1371/journal.pone.0063536 https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0063536&type=printable |
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