Genetics of dystonia: What's known? What's new? What's next?

Movement Disorders

Volumn 28, Issue 7, 2013, Pages 899-905

  Lohmann, Katja ^a   Klein, Christine ^a  

^a UNIVERSITY OF LÜBECK   (Germany)

Author keywords

Dystonia; Exome sequencing; Gene; Pathways; Penetrance

Indexed keywords

DOPAMINE; GUANOSINE TRIPHOSPHATE CYCLOHYDROLASE I; ION CHANNEL; SEPIAPTERIN REDUCTASE; TYROSINE 3 MONOOXYGENASE;

ADOLESCENT; ADULT; AUTOSOMAL DOMINANT INHERITANCE; AUTOSOMAL RECESSIVE INHERITANCE; CELL CYCLE; CELL TRANSPORT; CLINICAL FEATURE; CYTOSKELETON; DETOXIFICATION; DYSKINESIA; DYSTONIA; ENERGY METABOLISM; EXOME; GENE LOCUS; GENE MUTATION; GENE SEQUENCE; GENETIC RISK; GENETIC SUSCEPTIBILITY; HUMAN; INVOLUNTARY MOVEMENT; MYOCLONUS; ONSET AGE; PARKINSONISM; PATHOGENESIS; PHENOTYPE; PRIORITY JOURNAL; REVIEW; RISK FACTOR; SIGNAL TRANSDUCTION; TRANSCRIPTION REGULATION; X CHROMOSOMAL INHERITANCE;

EID: 84880784410     PISSN: 08853185     EISSN: 15318257     Source Type: Journal    
DOI: 10.1002/mds.25536     Document Type: Review

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