Scott et al., 2017
- Nuclear/cytoplasmic transport defects in BBS6 underlie congenital heart disease through perturbation of a chromatin remodeling protein.
PLoS Genetics
13:e1006936
Full text @ PLoS Genet.
Target | Reagent |
---|---|
mkks | MO3-mkks |
smarcc1a | MO2-smarcc1a |
MO3-smarcc1a |