Rare sequence variants in ANO3 and GNAL in a primary torsion dystonia series and controls

Movement Disorders

Volumn 29, Issue 1, 2014, Pages 143-147

  Zech, Michael ^a,b   Gross, Nadine ^a   Jochim, Angela ^a   Castrop, Florian ^a   Kaffe, Maria ^a,b   Dresel, Christian ^a   Lichtner, Peter ^b,c   Peters, Annette ^b   Gieger, Christian ^b   Meitinger, Thomas ^b,c   Haslinger, Bernhard ^a   Winkelmann, Juliane ^a,b,c,d,e  

^a TECHNICAL UNIVERSITY OF MUNICH   (Germany)

^b INSTITUTE OF EPIDEMIOLOGY   (Germany)

^c TECHNICAL UNIVERSITY OF MUNICH   (Germany)

^d STANFORD UNIVERSITY SCHOOL OF MEDICINE   (United States)

^e Technische Universität München Munich Cluster for Systems Neurology   (Germany)

Author keywords

ANO3; Dystonia; Gene; GNAL; Rare variants

Indexed keywords

ANOCTAMIN 3; GNAL PROTEIN; PROTEIN; UNCLASSIFIED DRUG;

ADULT; AGED; ARTICLE; CONTROLLED STUDY; EXON; FEMALE; GENETIC VARIABILITY; HIGH RESOLUTION MELTING ANALYSIS; HUMAN; MAJOR CLINICAL STUDY; MALE; MIDDLE AGED; PATHOGENESIS; POPULATION; PRIORITY JOURNAL; TORSION DYSTONIA;

ANO3; DYSTONIA; GENE; GNAL; RARE VARIANTS;

ADULT; AGED; AGED, 80 AND OVER; CHLORIDE CHANNELS; DYSTONIA MUSCULORUM DEFORMANS; FEMALE; GTP-BINDING PROTEIN ALPHA SUBUNITS; HUMANS; MALE; MIDDLE AGED; MUTATION, MISSENSE; YOUNG ADULT;

EID: 84892921433     PISSN: 08853185     EISSN: 15318257     Source Type: Journal    
DOI: 10.1002/mds.25715     Document Type: Article

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