Cite
HARVARD Citation
Lopez, E. et al. (2016). Mutations in MYT1, encoding the myelin transcription factor 1, are a rare cause of OAVS. Journal of medical genetics. 53 (11), pp. 752-760. [Online].
This is an interim version of our Electronic Legal Deposit Catalogue-eJournals and eBooks while we continue to recover from a cyber-attack.
Lopez, E. et al. (2016). Mutations in MYT1, encoding the myelin transcription factor 1, are a rare cause of OAVS. Journal of medical genetics. 53 (11), pp. 752-760. [Online].