Communicated by Robert Desnick
An activated 5′ cryptic splice site in the human ALG3 gene generates a premature termination codon insensitive to nonsense-mediated mRNA decay in a new case of congenital disorder of glycosylation type Id (CDG-Id)†
Version of Record online: 31 MAR 2004
Copyright © 2004 Wiley-Liss, Inc.
Volume 23, Issue 5, pages 477–486, May 2004
How to Cite
Denecke, J., Kranz, C., Kemming, D., Koch, H.-G. and Marquardt, T. (2004), An activated 5′ cryptic splice site in the human ALG3 gene generates a premature termination codon insensitive to nonsense-mediated mRNA decay in a new case of congenital disorder of glycosylation type Id (CDG-Id). Hum. Mutat., 23: 477–486. doi: 10.1002/humu.20026
- Issue online: 31 MAR 2004
- Version of Record online: 31 MAR 2004
- Manuscript Accepted: 22 DEC 2003
- Manuscript Received: 31 JUL 2003
- Innovative Medizinische Forschung. Grant Number: DE110325
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