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Epigenetic modifications in trinucleotide repeat diseases

โœ Scribed by Evans-Galea, Marguerite V.; Hannan, Anthony J.; Carrodus, Nissa; Delatycki, Martin B.; Saffery, Richard


Book ID
121181698
Publisher
Elsevier Science
Year
2013
Tongue
English
Weight
639 KB
Volume
19
Category
Article
ISSN
1471-4914

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โœ Ruth H. Walker; Paul F. Good; P. Shashidharan ๐Ÿ“‚ Article ๐Ÿ“… 2003 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 318 KB

## Abstract A mutation of the __DYT1__ gene, which codes for torsinA, has been identified as a cause of autosomal dominantly inherited dystonia. The function of torsinA is not yet known, but it is found throughout the central nervous system and has been identified in Lewy bodies in Parkinson's dise