No evidence of allelic heterogeneity in the DYT1 gene of European patients with early onset torsion dystonia.

Journal of medical genetics

Volumn 38, Issue 10, 2001, Pages

  Tuffery Giraud, S ^a   Cavalier, L ^a   Roubertie, A ^a   Guittard, C ^a   Carles, S ^a   Calvas, P ^a   Echenne, B ^a   Coubes, P ^a   Claustres, M ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

CARRIER PROTEIN; CHAPERONE; DYT1 PROTEIN, HUMAN;

ADOLESCENT; ADULT; ALLELE; CHILD; EUROPE; EXON; FEMALE; GENE DELETION; GENETIC HETEROGENEITY; GENETICS; GENOTYPE; HUMAN; JEW; LETTER; MALE; NUCLEOTIDE SEQUENCE; ONSET AGE; PATHOPHYSIOLOGY; PHENOTYPE; PRESCHOOL CHILD; TORSION DYSTONIA;

ADOLESCENT; ADULT; AGE OF ONSET; ALLELES; CARRIER PROTEINS; CHILD; CHILD, PRESCHOOL; DNA MUTATIONAL ANALYSIS; DYSTONIA MUSCULORUM DEFORMANS; EUROPE; EXONS; FEMALE; GENETIC HETEROGENEITY; GENOTYPE; HUMANS; JEWS; MALE; MOLECULAR CHAPERONES; PHENOTYPE; SEQUENCE DELETION;

MLCS; MLOWN;

EID: 0035491320     PISSN: None     EISSN: 14686244     Source Type: Journal    
DOI: 10.1136/jmg.38.10.e35     Document Type: Letter

References (0)