Lahrouchi et al., 2019
- Homozygous frameshift mutations in FAT1 cause a syndrome characterized by colobomatous-microphthalmia, ptosis, nephropathy and syndactyly.
Nature communications
10:1180
Full text @ Nat. Commun.
Target | Reagent |
---|---|
fat1a | MO2-fat1a |
fat4 | MO1-fat4 |