Severe impairment of male reproductive organ development in a low SMN expressing mouse model of spinal muscular atrophy
Author:
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/srep20193.pdf
Reference70 articles.
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2. Cho, S. & Dreyfuss, G. A degron created by SMN2 exon 7 skipping is a principal contributor to spinal muscular atrophy severity. Genes Dev 24, 438–442, 10.1101/gad.1884910 (2010).
3. Seo, J., Howell, M. D., Singh, N. N. & Singh, R. N. Spinal muscular atrophy: An update on therapeutic progress. Biochimica Et Biophysica Acta-Molecular Basis of Disease 1832, 2180–2190, 10.1016/j.bbadis.2013.08.005 (2013).
4. Boyer, J. G., Ferrier, A. & Kothary, R. More than a bystander: the contributions of intrinsic skeletal muscle defects in motor neuron diseases. Frontiers in physiology 4, 356, 10.3389/fphys.2013.00356 (2013).
5. Heier, C. R., Satta, R., Lutz, C. & DiDonato, C. J. Arrhythmia and cardiac defects are a feature of spinal muscular atrophy model mice. Human Molecular Genetics 19, 3906–3918, 10.1093/hmg/ddq330 (2010).
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