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Scaled-down genetic analysis of myotonic dystrophy type 1 and type 2
Types 1 and 2 myotonic dystrophy are neuromuscular disorders caused by genomic expansions of simple sequence repeats. These mutations are unstable in somatic cells, which leads to an age-dependent increase of expansion length. Studies to determine whether changes in repeat size may influence disease...
Tallennettuna:
| Päätekijät: | , , , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2009
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2767455/ https://ncbi.nlm.nih.gov/pubmed/19713112 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nmd.2009.07.012 |
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