Mapping disease-related missense mutations in the immunoglobulin-like fold domain of lamin A/C reveals novel genotype–phenotype associations for laminopathies
Article first published online: 26 DEC 2013
© 2013 Wiley Periodicals, Inc.
Proteins: Structure, Function, and Bioinformatics
Volume 82, Issue 6, pages 904–915, June 2014
How to Cite
Scharner, J., Lu, H.-C., Fraternali, F., Ellis, J. A. and Zammit, P. S. (2014), Mapping disease-related missense mutations in the immunoglobulin-like fold domain of lamin A/C reveals novel genotype–phenotype associations for laminopathies. Proteins, 82: 904–915. doi: 10.1002/prot.24465
- Issue published online: 17 MAY 2014
- Article first published online: 26 DEC 2013
- Accepted manuscript online: 9 NOV 2013 02:56AM EST
- Manuscript Accepted: 21 OCT 2013
- Manuscript Revised: 11 OCT 2013
- Manuscript Received: 1 JUL 2013
- OPTISTEM through the European Union 7th Framework Programme supported JS . Grant Number: 223098
- Medical Research Council . Grant Number: (G1100193)
- The Medical Research Council under which this work was initiated . Grant Number: G0700307
- British Heart Foundation . Grant Number: NH/12/2/29427. The Zammit lab also acknowledges financial support from the Muscular Dystrophy Campaign, Association Francaise contre les Myopathies and BIODESIGN (contract 262948-2) through the European Union 7th Framework Programme
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