Trinucleotide repeat expansion in SCA 17/TBP in white patients with Huntington's disease-like phenotype

Authors :: Bauer, P.
Laccone, F.
Rolfs, A.
Wullner, U.
Bosch, S.
Peters, H.
Liebscher, S.
Scheible, M.
Epplen, J.T.
Weber, B.H.F.
Holinski-Feder, E.
Weirich-Schwaiger, H.
Morris-Rosendahl, D.J.
Andrich, J.
Riess, O.
Source :: Journal of Medical Genetics. March 2004, Vol. 41 Issue 3, p230, 3 p.
Publication Year :: 2004
Abstract: J Med Genet 2004;41:230-232. doi: 10.1136/jmg.2003.015602 Huntington's disease (HD) is characterized by movement abnormalities and psychiatric symptoms. Prominent features include choreiform movements, dysarthria, ataxia, depression, dementia, and personality changes. The [...]

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