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

Research output: Contribution to journal › Journal article › Research › peer-review

Standard

The D216H variant in the DYT1 gene: a susceptibility factor for dystonia in familial cases? / Brüggemann, N; Kock, N; Lohmann, K; König, I R; Rakovic, A; Hagenah, J; Schmidt, A.; Ziegler, A; Jabusch, H C; Siebner, H; Altenmüller, E; Münchau, A; Klein, C.

In: Neurology, Vol. 72, No. 16, 2009, p. 1441-3.

Research output: Contribution to journal › Journal article › Research › peer-review

Harvard

Brüggemann, N, Kock, N, Lohmann, K, König, IR, Rakovic, A, Hagenah, J, Schmidt, A, Ziegler, A, Jabusch, HC, Siebner, H, Altenmüller, E, Münchau, A & Klein, C 2009, 'The D216H variant in the DYT1 gene: a susceptibility factor for dystonia in familial cases?', Neurology, vol. 72, no. 16, pp. 1441-3. https://doi.org/10.1212/WNL.0b013e3181a1861e

APA

Brüggemann, N., Kock, N., Lohmann, K., König, I. R., Rakovic, A., Hagenah, J., Schmidt, A., Ziegler, A., Jabusch, H. C., Siebner, H., Altenmüller, E., Münchau, A., & Klein, C. (2009). The D216H variant in the DYT1 gene: a susceptibility factor for dystonia in familial cases? Neurology, 72(16), 1441-3. https://doi.org/10.1212/WNL.0b013e3181a1861e

Vancouver

Brüggemann N, Kock N, Lohmann K, König IR, Rakovic A, Hagenah J et al. The D216H variant in the DYT1 gene: a susceptibility factor for dystonia in familial cases? Neurology. 2009;72(16):1441-3. https://doi.org/10.1212/WNL.0b013e3181a1861e

Author

Brüggemann, N ; Kock, N ; Lohmann, K ; König, I R ; Rakovic, A ; Hagenah, J ; Schmidt, A. ; Ziegler, A ; Jabusch, H C ; Siebner, H ; Altenmüller, E ; Münchau, A ; Klein, C. / The D216H variant in the DYT1 gene: a susceptibility factor for dystonia in familial cases?. In: Neurology. 2009 ; Vol. 72, No. 16. pp. 1441-3.

Bibtex

@article{3007cc10aac911df928f000ea68e967b,

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

abstract = "Udgivelsesdato: 2009-Apr",

author = "N Br{\"u}ggemann and N Kock and K Lohmann and K{\"o}nig, {I R} and A Rakovic and J Hagenah and A. Schmidt and A Ziegler and Jabusch, {H C} and H Siebner and E Altenm{\"u}ller and A M{\"u}nchau and C Klein",

note = "Keywords: 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",

year = "2009",

doi = "10.1212/WNL.0b013e3181a1861e",

language = "English",

volume = "72",

pages = "1441--3",

journal = "Neurology",

issn = "0028-3878",

publisher = "Lippincott Williams & Wilkins",

number = "16",