Abnormalities of motor function, transcription and cerebellar structure in mouse models ofTHAP1dystonia-Reference-Cited by-同舟云学术

Abnormalities of motor function, transcription and cerebellar structure in mouse models ofTHAP1dystonia

Published:2015-09-16 Issue:25 Volume:24 Page:7159-7170
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Hum. Mol. Genet.

Author:

Ruiz Marta,Perez-Garcia Georgina,Ortiz-Virumbrales Maitane,Méneret Aurelie,Morant Andrika,Kottwitz Jessica,Fuchs Tania,Bonet Justine,Gonzalez-Alegre Pedro,Hof Patrick R.,Ozelius Laurie J.,Ehrlich Michelle E.

Funder

Bachmann-Strauss Dystonia and Parkinson

Foundation

Dystonia Medical Research Foundation

National Institutes of

Health

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/24/25/7159/17262221/ddv384.pdf

Reference50 articles.

1. Emerging common molecular pathways for primary dystonia

2. Hereditary dystonia as a neurodevelopmental circuit disorder: Evidence from neuroimaging

3. Mutations in the THAP1 gene are responsible for DYT6 primary torsion dystonia

4. Dimerization of the DYT6 dystonia protein, THAP1, requires residues within the coiled-coil domain

5. The THAP domain: a novel protein motif with similarity to the DNA-binding domain of P element transposase

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