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The D216H variant in the DYT1 gene: a susceptibility factor for dystonia in familial cases?

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Authors:
  • Brüggemann, N ;
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  • Kock, N ;
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  • Lohmann, K ;
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  • König, I R ;
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  • Rakovic, A ;
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  • Hagenah, J ;
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  • Schmidt, A. ;
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  • Ziegler, A ;
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  • Jabusch, H C ;
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  • Siebner, H ;
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  • Altenmüller, E ;
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  • Münchau, A ;
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  • Klein, C
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DOI:
10.1212/wnl.0b013e3181a1861e
Abstract:
Udgivelsesdato: 2009-Apr
Type:
Journal article
Language:
English
Published in:
Neurology, 2009, Vol 72, Issue 16, p. 1441-3
Keywords:
Journal Article; Research Support, Non-U.S. Gov't; Adult; Aged; Blepharospasm; DNA Mutational Analysis; Dystonia; Dystonic Disorders; Family Health; Female; Gene Frequency; Genetic Predisposition to Disease; Genetic Testing; Genetic Variation; Genotype; Germany; Humans; Male; Middle Aged; Molecular Chaperones; Penetrance; Polymorphism, Genetic; Torticollis
Main Research Area:
Medical science
Publication Status:
Published
Review type:
Peer Review
Submission year:
2009
Scientific Level:
Scientific
ID:
110377324

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