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FUS pathology in basophilic inclusion body disease

โœ Scribed by David G. Munoz; Manuela Neumann; Hirofumi Kusaka; Osamu Yokota; Kenji Ishihara; Seishi Terada; Shigetoshi Kuroda; Ian R. Mackenzie


Publisher
Springer-Verlag
Year
2009
Tongue
English
Weight
593 KB
Volume
118
Category
Article
ISSN
0001-6322

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TorsinA immunoreactivity in inclusion bo
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