Ansar et al., 2020
- Biallelic variants in PSMB1 encoding the proteasome subunit β6 cause impairment of proteasome function, microcephaly, intellectual disability, developmental delay and short stature.
Human molecular genetics
29(7):1132-1143
Full text @ Hum. Mol. Genet.
Target | Reagent |
---|---|
psmb1 | CRISPR1-psmb1 |
CRISPR2-psmb1 | |
CRISPR3-psmb1 |