Novel THAP1 gene mutations in patients with primary dystonia from Southwest China

Journal of the Neurological Sciences

Volumn 309, Issue 1-2, 2011, Pages 63-67

  Song, Wei ^a   Chen, Yongping ^a   Huang, Rui ^a   Chen, Ke ^a   Pan, Pinglei ^a   Yang, Yuan ^a   Shang, Hui Fang ^a  

^a SICHUAN UNIVERSITY   (China)

Author keywords

Clinical feature; DYT6 THAP1 gene; Mutation; Primary dystonia

Indexed keywords

ALANINE; APOPTOSIS REGULATORY PROTEIN; CYSTEINE; DYT1 PROTEIN; GLYCINE; HALOPERIDOL; NEUROPEPTIDE; PHENYLALANINE; THAP1 PROTEIN; UNCLASSIFIED DRUG;

ADULT; AMINO ACID SUBSTITUTION; ARTICLE; CERVICAL DYSTONIA; CHILD; CHINA; DYSARTHRIA; DYSTONIA; EXON; FEMALE; FOCAL DYSTONIA; GENE FREQUENCY; GENE INSERTION; GENE MUTATION; GENE SEQUENCE; GENETIC SCREENING; HETEROZYGOSITY; HUMAN; MAJOR CLINICAL STUDY; MALE; MEIGE SYNDROME; MISSENSE MUTATION; NUCLEOTIDE SEQUENCE; PRESCHOOL CHILD; PRIMARY DYSTONIA; PRIORITY JOURNAL; SYMPTOM;

ADULT; AGED; APOPTOSIS REGULATORY PROTEINS; ASIAN CONTINENTAL ANCESTRY GROUP; CHINA; COHORT STUDIES; DNA-BINDING PROTEINS; DYSTONIC DISORDERS; FEMALE; HUMANS; MALE; MIDDLE AGED; MUTATION, MISSENSE; NUCLEAR PROTEINS; YOUNG ADULT;

EID: 80052388330     PISSN: 0022510X     EISSN: 18785883     Source Type: Journal    
DOI: 10.1016/j.jns.2011.07.023     Document Type: Article

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