DOI:
10.1055/s-00000041
Neuropediatrics
LinksClose Window
References
Pan T-C, Zhang R-Z, Sudano DG, Marie SK, Bönnemann CG, Chu M-L.
New molecular mechanism for Ullrich congenital muscular dystrophy: a heterozygous in-frame deletion in the COL6A1 gene causes a severe phenotype.
Am J Hum Genet 2003;
73 (02) 355-369
Access:
Access:
We do not assume any responsibility for the contents of the web pages of other providers.