Mutation of senataxin alters disease-specific transcriptional networks in patients with ataxia with oculomotor apraxia type 2

Human Molecular Genetics

Volumn 23, Issue 18, 2014, Pages 4758-4769

  Fogel, Brent L ^a   Cho, Ellen ^a   Wahnich, Amanda ^a   Gao, Fuying ^a   Becherel, Olivier J ^c   Wang, Xizhe ^a   Fike, Francesca ^b   Chen, Leslie ^a   Criscuolo, Chiara ^d   De Michele, Giuseppe ^d   Filla, Alessandro ^d   Collins, Abigail ^e   Hahn, Angelika F ^f   Gatti, Richard A ^b   Konopka, Genevieve ^g   Perlman, Susan ^a   Lavin, Martin F ^c   Geschwind, Daniel H ^a,b   Coppola, Giovanni ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

^c UNIVERSITY OF QUEENSLAND   (Australia)

^d UNIVERSITY OF NAPLES FEDERICO II   (Italy)

^e CHILDREN S HOSPITAL COLORADO   (United States)

^f UNIVERSITY OF WESTERN ONTARIO   (Canada)

^g UNIVERSITY OF TEXAS SOUTHWESTERN MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DNA HELICASE; RNA HELICASE; SETX PROTEIN, HUMAN; SETX PROTEIN, MOUSE;

AMYOTROPHIC LATERAL SCLEROSIS; ANIMAL; ATAXIA; BLOOD; CELL LINE; CEREBELLUM; COGAN SYNDROME; DNA MICROARRAY; FIBROBLAST; GENE EXPRESSION REGULATION; GENE REGULATORY NETWORK; GENETICS; HUMAN; METABOLISM; MOUSE; MUTATION; PATHOLOGY; PHENOTYPE; SEQUENCE ANALYSIS;

AMYOTROPHIC LATERAL SCLEROSIS; ANIMALS; ATAXIA; CELL LINE; CEREBELLUM; COGAN SYNDROME; DNA HELICASES; FIBROBLASTS; GENE EXPRESSION REGULATION; GENE REGULATORY NETWORKS; HUMANS; MICE; MUTATION; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; PHENOTYPE; RNA HELICASES; SEQUENCE ANALYSIS, RNA;

EID: 84906661754     PISSN: 09646906     EISSN: 14602083     Source Type: Journal    
DOI: 10.1093/hmg/ddu190     Document Type: Article

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