DOI:
10.1055/s-00000041
Neuropediatrics
LinksClose Window
References
Labelle-Dumais C, Dilworth DJ, Harrington EP et al.
COL4A1 mutations cause, ocular dysgenesis, neuronal localisation defects and myopathy in mice and Walker-Warburg Syndrome in humans.
PLoS Genet 2011;
7 (05) e1002062
DOI: 10.1371/journal.pgen.10020622011.
Access:
Access:
We do not assume any responsibility for the contents of the web pages of other providers.