A Skeletal Muscle Model of Infantile-onset Pompe Disease with Patient-specific iPS Cells
Author:
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/s41598-017-14063-y.pdf
Reference60 articles.
1. Kishnani, P. S. & Howell, R. R. Pompe disease in infants and children. J. Pediatr. 144, S35–43, https://doi.org/10.1016/j.jpeds.2004.01.053 (2004).
2. Kishnani, P. S. et al. Pompe disease diagnosis and management guideline. Genet. Med. 8, 267–288, 10.109701.gim.0000218152.87434.f3 (2006).
3. van den Hout, H. M. et al. The natural course of infantile Pompe’s disease: 20 original cases compared with 133 cases from the literature. Pediatrics 112, 332–340 (2003).
4. Kishnani, P. S. et al. A retrospective, multinational, multicenter study on the natural history of infantile-onset Pompe disease. J. Pediatr. 148, 671–676, https://doi.org/10.1016/j.jpeds.2005.11.033 (2006).
5. Winkel, L. P. et al. The natural course of non-classic Pompe’s disease; a review of 225 published cases. J. Neurol. 252, 875–884, https://doi.org/10.1007/s00415-005-0922-9 (2005).
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