Genetic issues in the diagnosis of dystonias

Frontiers in Neurology

Volumn 4 APR, Issue , 2013, Pages

  Petrucci, Simona ^a,b   Valente, Enza Maria ^a,c  

^a CASA SOLLIEVO DELLA SOFFERENZA HOSPITAL   (Italy)

^b SAPIENZA UNIVERSITY OF ROME   (Italy)

^c UNIVERSITY OF SALERNO   (Italy)

Author keywords

Counseling; Diagnosis; Dystonia; Dyt1; Dyt6; Genetic; Non motor; Phenotype

Indexed keywords

BETA TUBULIN; CALCIUM ACTIVATED CHLORIDE CHANNEL; CARRIER PROTEIN; GUANINE NUCLEOTIDE BINDING PROTEIN; TORSIN 1A; UNCLASSIFIED DRUG; ZINC FINGER PROTEIN;

ANO3 GENE; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; AUTOSOMAL RECESSIVE INHERITANCE; CIZ1 GENE; DYSTONIA; ENVIRONMENTAL FACTOR; GENE; GENE IDENTIFICATION; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENETIC COUNSELING; GNAL GENE; HEREDITY; HUMAN; MOLECULAR DIAGNOSIS; PATHOGENESIS; THAP1 GENE; TOR1A GENE; TORSION DYSTONIA; TUBB4A GENE;

EID: 84878696432     PISSN: None     EISSN: 16642295     Source Type: Journal    
DOI: 10.3389/fneur.2013.00034     Document Type: Article

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