Frequency of DYT1 mutation in early-onset primary dystonia in Italian patients

Movement Disorders

Volumn 17, Issue 2, 2002, Pages 407-408

  Zorzi, Giovanna ^a   Garavaglia, Barbara ^a   Invernizzi, Federica ^a   Girotti, Floriano ^a   Soliveri, Paola ^a   Zeviani, Massimo ^a   Angelini, Lucia ^a   Nardocci, Nardo ^a  

^a DEPARTMENT OF NEUROSURGERY   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

BINDING PROTEIN; TORSIN A; UNCLASSIFIED DRUG;

ADOLESCENT; ADULT; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CHILD; CLINICAL ARTICLE; CONTROLLED STUDY; DYSTONIA; FACE MUSCLE; FEMALE; GENE DELETION; GENETIC COUNSELING; GENETIC HETEROGENEITY; GENETIC SCREENING; GENOTYPE PHENOTYPE CORRELATION; HUMAN; ITALY; MALE; MUTATIONAL ANALYSIS; ONSET AGE; PHENOTYPIC VARIATION; PRIORITY JOURNAL;

ADOLESCENT; ADULT; CARRIER PROTEINS; CHILD; CHILD, PRESCHOOL; DYSTONIC DISORDERS; FEMALE; GENE FREQUENCY; GENETICS, POPULATION; HUMANS; ITALY; MALE; MOLECULAR CHAPERONES; MUTATION;

EID: 0036523854     PISSN: 08853185     EISSN: None     Source Type: Journal    
DOI: 10.1002/mds.10045     Document Type: Article

References (10)

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