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SCA17 homozygote showing Huntington's disease-like phenotype

✍ Scribed by Yasuko Toyoshima; Mitsunori Yamada; Osamu Onodera; Mitsuteru Shimohata; Chikanori Inenaga; Nobuya Fujita; Masahiro Morita; Shoji Tsuji; Hitoshi Takahashi


Publisher
John Wiley and Sons
Year
2004
Tongue
English
Weight
358 KB
Volume
55
Category
Article
ISSN
0364-5134

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Phenotypic features of Huntington's dise
✍ Ruth H. Walker; Joseph Jankovic; Elizabeth O'Hearn; Russell L. Margolis πŸ“‚ Article πŸ“… 2003 πŸ› John Wiley and Sons 🌐 English βš– 59 KB

## Abstract Huntington's disease‐like 2 is an autosomal dominantly inherited disorder due to an expansion of trinucleotide repeats. It resembles classic Huntington's disease in clinical phenotype, inheritance pattern, and neuropathological features. We highlight the clinical features of this disord