Lack of association with TorsinA haplotype in German patients with sporadic dystonia

Neurology

Volumn 66, Issue 6, 2006, Pages 951-952

  Hague, S ^a   Klaffke, S ^a   Clarimon, J ^b   Hemmer, B ^c   Singleton, A ^b   Kupsch, A ^d   Bandmann, O ^a,e  

^a UNIVERSITY OF SHEFFIELD   (United Kingdom)

^b Laboratory of Neurogenetics   (United States)

^c Department of Neurology ^*  (Germany)

^d CHARITÉ UNIVERSITÄTSMEDIZIN BERLIN   (Germany)

^e UNIVERSITY OF SHEFFIELD   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ALLELE; ARTICLE; BLEPHAROSPASM; CAUCASIAN; CONTROLLED STUDY; DYSTONIA; FEMALE; GENE LINKAGE DISEQUILIBRIUM; GENETIC POLYMORPHISM; GENETIC VARIABILITY; GENOTYPE; GERMANY; HAPLOTYPE; HUMAN; MAJOR CLINICAL STUDY; MALE; MUSCLE CRAMP; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; TORTICOLLIS; AGED; COMPARATIVE STUDY; GENETIC LINKAGE; GENETICS; MIDDLE AGED;

CHAPERONE; DYT1 PROTEIN, HUMAN;

ADULT; AGED; ALLELES; DYSTONIC DISORDERS; FEMALE; GERMANY; HAPLOTYPES; HUMANS; LINKAGE (GENETICS); MALE; MIDDLE AGED; MOLECULAR CHAPERONES;

EID: 33645827756     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/01.wnl.0000203344.43342.18     Document Type: Article

References (5)

1. Ozelius LJ, Hewett JW, Page CE, et al. The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein. Nat Genet 1997;17:40-48.
2. Clarimon J, Asgeirsson H, Singleton A, et al. TorsinA haplotype predisposes to idiopathic dystonia. Ann Neurol 2005;57:765-767.
3. Peltonen L, Palotie A, Lange K. Use of population isolates for mapping complex traits. Nat Rev Genet 2000;1:182-190.
4. Stephens M, Smith N, Donnely P. A new statistical method for haplotype reconstruction from population data. Am J Hum Genet 2001;68:978-989.
5. Stephens M, Scheet P. Accounting for the delay of linkage disequilibrium in haplotype inference and missing data manipulation. Am J Hum Genet 2005;76:449-462.