Deciphering transcription dysregulation in FSH muscular dystrophy
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
http://www.nature.com/articles/jhg201274.pdf
Reference100 articles.
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2. Matsumura, T., Goto, K., Yamanaka, G., Lee, J., Zhang, C., Hayashi, Y. K. et al. Chromosome 4q;10q translocations; comparison with different ethnic populations and FSHD patients. BMC Neurol. 2, 7 (2002).
3. Lemmers, R. J., van der Vliet, P. J., van der Gaag, K. J., Zuniga, S., Frants, R. R., de Knijff, P. et al. Worldwide population analysis of the 4q and 10q subtelomeres Identifies only four discrete interchromosomal sequence transfers in human evolution. Am. J. Hum. Genet. 86, 364–377 (2010).
4. Kowaljow, V., Marcowycz, A., Ansseau, E., Conde, C. B., Sauvage, S., Matteotti, C. et al. The DUX4 gene at the FSHD1A locus encodes a pro-apoptotic protein. Neuromuscul. Disord. 17, 611–623 (2007).
5. Lemmers, R. J., van der Vliet, P. J., Klooster, R., Sacconi, S., Camano, P., Dauwerse, J. G. et al. A unifying genetic model for facioscapulohumeral muscular dystrophy. Science 329, 1650–1653 (2010).
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