DUX4, a candidate gene for facioscapulohumeral muscular dystrophy, causes p53-dependent myopathy in vivo

Author:

Wallace Lindsay M.,Garwick Sara E.,Mei Wenyan,Belayew Alexandra,Coppee Frederique,Ladner Katherine J.,Guttridge Denis,Yang Jing,Harper Scott Q.

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Reference62 articles.

1. Prevalence of rare diseases: bibliographic data http://www.orpha.net/orphacom/cahiers/docs/GB/Prevalence_of_rare_diseases_by_alphabetical_list.pdf 2010

2. Severe phenotype in infantile facioscapulohumeral muscular dystrophy;Klinge;Neuromuscul Disord,2006

3. FSHD associated DNA rearrangements are due to deletions of integral copies of a 3.2 kb tandem repeated unit;van Deutekom;Hum Mol Genet,1993

4. Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy;Wijmenga;Nat Genet,1992

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