- Mig12, a novel Opitz syndrome gene product partner, is expressed in the embryonic ventral midline and co-operates with Mid1 to bundle and stabilize microtubulesCaterina Berti
Telethon Institute of Genetics and Medicine, 80131 Naples, Italy
BMC Cell Biol 5:9. 2004..Mid1 acts as an E3 ubiquitin ligase, regulating PP2A degradation on microtubules...
- X-linked Opitz syndrome: novel mutations in the MID1 gene and redefinition of the clinical spectrumFrancesca De Falco
Telethon Institute of Genetics and Medicine, Naples, Italy
Am J Med Genet A 120:222-8. 2003..The low frequency of mutations in MID1 and the high variability of the phenotype suggest the involvement of other genes in the OS phenotype...