This is a preview of subscription content, access via your institution
Relevant articles
Open Access articles citing this article.
-
In silico and in vivo splicing analysis of MLH1 and MSH2 missense mutations shows exon- and tissue-specific effects
BMC Genomics Open Access 22 September 2006
-
Multi-exon deletions of the FBN1gene in Marfan syndrome
BMC Medical Genetics Open Access 24 October 2001
Access options
Subscribe to this journal
Receive 12 print issues and online access
$209.00 per year
only $17.42 per issue
Rent or buy this article
Prices vary by article type
from$1.95
to$39.95
Prices may be subject to local taxes which are calculated during checkout
References
Reed, R., Genet Dev. 6, 215–220 (1996).
Dietz, H.C. et al. Nature 352, 337–339 (1991).
Dietz, H.C. & Pyeritz, R.E. Hum. Mol. Genet. 4, 1799–1809 (1995).
Liu, W. et al. Hum. Mol. Genet. 5, 1581–1587 (1996).
Kanzaki, T. et al. Cell 61, 1051–1061 (1990).
Tian, H. & Kole, R. Mol. Cell. Biol. 15, 6291–6298 (1995).
Nijbroek, G. et al. Am. J. Hum. Genet. 57, 8–21 (1995).
Dietz, H.C. et al. Science 259, 680–683 (1993).
Ruskin, B., Krainer, A.R., Maniatis, T. & Green, M.R. Cell 38, 317–331 (1984).
Chen, B. & Przybyla, A.E. BioTechniques 17, 657–659 (1994).
Database at the Institute of Medical Genetics in Cardiff (http://www.cf.ac.uk/uwcm/mg/hgmdO.html) (1996).
Krawczak, M., Reiss, J. & Cooper, D.N. Hum. Genet. 90, 41–54 (1992).
Dietz, H.C. & Kendzior, R.J. Jr. Nature Genet. 8, 183–188 (1994).
Santisteban, I. et al. Hum. Mol. Genet. 4, 2081–2087 (1995).
Belgrader, P. & Maquat, L.E. Mol. Cell Biol. 14, 6326–6336 (1994).
Berg, M.A., Guevara-Aguirre, J., Rosenbloom, A.L., Rosenfeld, R.G. & Francke, U. Hum. Mut. 1, 24–34 (1992).
Li, X., Park, W.J., Pyeritz, R.E. & Jabs, E.W. Nature Genet. 9, 232–233 (1995).
Milland, J., Christiansen, D., Thorley, B.R., McKenzie, I.F. & Loveland, B.E. Eur. J. Biochem. 238, 221–230 (1995).
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
About this article
Cite this article
Liu, W., Qian, C. & Francke, U. Silent mutation induces exon skipping of fibrillin-1 gene in Marfan syndrome. Nat Genet 16, 328–329 (1997). https://doi.org/10.1038/ng0897-328
Issue Date:
DOI: https://doi.org/10.1038/ng0897-328
This article is cited by
-
Spectrum of CREBBP mutations in Indian patients with Rubinstein-Taybi syndrome
Journal of Biosciences (2010)
-
Expression of Glutathione Reductase Splice Variants in Human Tissues
Biochemical Genetics (2010)
-
Report on mutation in exon 15 of the APC gene in a case of brain metastasis
Journal of Neuro-Oncology (2010)
-
Alternative RNA splicing in expression of the glutathione synthetase gene in human cells
Molecular Biology Reports (2010)
-
In silico and in vivo splicing analysis of MLH1 and MSH2 missense mutations shows exon- and tissue-specific effects
BMC Genomics (2006)