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Corrigendum for Nasim et al., Hum. Mol. Genet. 12 (11) 1337-1348.
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Human Molecular Genetics, 2003, Vol. 12, No. 15 1941
DOI: 10.1093/hmg/ddg201
© 2003 Oxford University Press

HnRNP G and Tra2ß: opposite effects on splicing matched by antagonism in RNA binding

M. Talat Nasim, Tatyana K. Chernova, Hasnin M. Chowdhury, Bai-Gong Yue and Ian C. Eperon

Human Molecular Genetics 12, 1337–1348 (2003)

The characterisation of a dystrophin gene rearrangement associated with X-linked dilated cardiomyopathy and used for some of the studies in the manuscript by Nasim et al. has been published:

Gualandi, G., Rimessi, P., Cardazzo, B., Toffolatti, L., Dunckley, M.G., Calzolari, E., Patarnello, T., Muntoni, F. and Ferlini, A. (2003) Genomic definition of a pure intronic dystrophin deletion responsible for an XLDC splicing mutation: in vitro mimicking and antisense modulation of the splicing abnormality. Gene, 311, 23–31.


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