Tetraplex formation by the progressive myoclonus epilepsy type-1 repeat: implications for instability in the repeat expansion diseases
Author:
Publisher
Wiley
Subject
Cell Biology,Genetics,Molecular Biology,Biochemistry,Structural Biology,Biophysics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1016/S0014-5793(01)02190-1/fullpdf
Reference44 articles.
1. Mutations in the Gene Encoding Cystatin B in Progressive Myoclonus Epilepsy (EPM1)
2. Unstable insertion in the 5′ flanking region of the cystatin B gene is the most common mutation in progressive myoclonus epilepsy type 1, EPM1
3. Dodecamer repeat expansion in cystatin B gene in progressive myoclonus epilepsy
4. Unstable minisatellite expansion causing recessively inherited myoclonus epilepsy, EPM1
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