Zivana Tezak and Paola Prandini contributed equally to this work
Clinical and molecular study in congenital muscular dystrophy with partial laminin α2 (LAMA2) deficiency†
Article first published online: 9 JAN 2003
© 2003 Wiley-Liss, Inc.
Volume 21, Issue 2, pages 103–111, February 2003
How to Cite
Tezak, Z., Prandini, P., Boscaro, M., Marin, A., Devaney, J., Marino, M., Fanin, M., Trevisan, C. P., Park, J., Tyson, W., Finkel, R., Garcia, C., Angelini, C., Hoffman, E. P. and Pegoraro, E. (2003), Clinical and molecular study in congenital muscular dystrophy with partial laminin α2 (LAMA2) deficiency. Hum. Mutat., 21: 103–111. doi: 10.1002/humu.10157
Communicated by Haig H. Kazazian, Jr.
- Issue published online: 9 JAN 2003
- Article first published online: 9 JAN 2003
- Manuscript Accepted: 24 OCT 2002
- Manuscript Received: 27 JUN 2002
- NIH (NINDS). Grant Number: RO1 2952
- University of Padova. Grant Number: 1462
- Telethon. Grant Number: TF0003Y019
- MURST. Grant Number: 2001068328001
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