A.K. Lampe and Y. Zou contributed equally to this work.
Exon skipping mutations in collagen VI are common and are predictive for severity and inheritance†
Version of Record online: 25 MAR 2008
© 2008 Wiley-Liss, Inc.
Volume 29, Issue 6, pages 809–822, June 2008
How to Cite
Lampe, A.K., Zou, Y., Sudano, D., O'Brien, K.K., Hicks, D., Laval, S.H., Charlton, R., Jimenez-Mallebrera, C., Zhang, R.-Z., Finkel, R.S., Tennekoon, G., Schreiber, G., van der Knaap, M.S., Marks, H., Straub, V., Flanigan, K.M., Chu, M.-L., Muntoni, F., Bushby, K.M.D. and Bönnemann, C.G. (2008), Exon skipping mutations in collagen VI are common and are predictive for severity and inheritance. Hum. Mutat., 29: 809–822. doi: 10.1002/humu.20704
Communicated by Maria Rita Passos-Bueno
- Issue online: 22 MAY 2008
- Version of Record online: 25 MAR 2008
- Manuscript Accepted: 18 NOV 2007
- Manuscript Received: 21 JUN 2007
- Muscular Dystrophy Campaign (MDC)
- National Specialist Commissioning Advisory Group (NSCAG)
- Muscular Dystrophy Association (MDA) USA. Grant Number: MDA3896
- National Institutes of Health (NIH)/National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS). Grant Number: R01AR051999
- National Institutes of Health (NIH). Grant Number: AR053251
- Pew Scholars Program in the Biomedical Sciences (CGB)
- Wellcome Entry level fellowship and Patrick Berthoud fellowship (AKL)
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