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DUX4L9 gene

Known as: DOUBLE HOMEOBOX 4-LIKE 9, double homeobox 4 like 9, DUX4L9 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Deregulation of IGF 2 BP 1-mRNP components during the differentiation of FSHD muscle cells
Facioscapulohumeral muscular dystrophy (FSHD) is caused by the misexpression of DUX4. Its homologue DUX4c is also induced in FSHD… 
2016
2016
Antisense strategies targeting DUX4 and DUX4c for the treatment of Facioscapulohumeral muscular dystrophy.
Review
2015
Review
2015
Bringing smiles to faces: Evidence‐based guidelines for facioscapulohumeral dystrophy
Facioscapulohumeral dystrophy (FSHD) is an autosomal dominant disorder and the third most common muscular dystrophy after… 
Review
2005
Review
2005
Characterization of DUX4c, a double homeobox gene located in a truncated and inverted D4Z4 element, and its expression in FSHD myoblasts.
Facioscapulohumeral muscular dystrophy (FSHD) is the third most frequent myopathy and affects 1/20,000 individuals. Muscle… 
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