טוען...
A novel GAA-repeat-expansion-based mouse model of Friedreich’s ataxia
Friedreich’s ataxia (FRDA) is an autosomal recessive neurodegenerative disorder caused by a GAA repeat expansion mutation within intron 1 of the FXN gene, resulting in reduced levels of frataxin protein. We have previously reported the generation of human FXN yeast artificial chromosome (YAC) transg...
שמור ב:
| הוצא לאור ב: | Dis Model Mech |
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| Main Authors: | , , , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
The Company of Biologists Limited
2015
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4348561/ https://ncbi.nlm.nih.gov/pubmed/25681319 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/dmm.018952 |
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