טוען...
Increased expression of the Hutchinson–Gilford progeria syndrome truncated lamin A transcript during cell aging
Most cases of the segmental progeroid syndrome, Hutchinson–Gilford progeria syndrome (HGPS), are caused by a de novo dominant mutation within a single codon of the LMNA gene. This mutation leads to the increased usage of an internal splice site that generates an alternative lamin A transcript with a...
שמור ב:
| Main Authors: | , , , |
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| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Nature Publishing Group
2009
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2986496/ https://ncbi.nlm.nih.gov/pubmed/19172989 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2008.270 |
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