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Mutational analysis of glycyl-tRNA synthetase (GARS) gene in Hirayama Disease
Sporadic juvenile muscular atrophy of the distal upper extremity or Hirayama's Disease (HD) and autosomal dominant motor distal neuronopathy/axonopathy (CMT2D/dSMA-V), produced by glycyl-tRNA synthetase (GARS) gene mutations, share some clinical features including: young age of onset, predilect...
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| Main Authors: | , , , , , , , |
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| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
2010
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2864347/ https://ncbi.nlm.nih.gov/pubmed/19412816 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/17482960902849823 |
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