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

N Brüggemann; N Kock; K Lohmann; I R König; A Rakovic; J Hagenah; A. Schmidt; A Ziegler; H C Jabusch; H Siebner; E Altenmüller; A Münchau; C Klein

doi:10.1212/wnl.0b013e3181a1861e

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

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

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

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