An intronic mutation in Chd7 creates a cryptic splice site, causing aberrant splicing in a mouse model of CHARGE syndrome
Jacqueline M Ogier, Benedicta D Arhatari, Marina R Carpinelli, Bradley K McColl, Michael A Wilson, Rachel A Burt
Scientific Reports | NATURE PUBLISHING GROUP | Published : 2018
This work was supported by the HEA Ring CRC, established and supported under the Cooperative Research Centres Program - an Australian Government Initiative; the Victorian State Government's Operational Infrastructure Support Program; the Australian Government's NHMRC IRIISS and the Garnet Passe and Rodney Williams Memorial Foundation (scholarship to JMO). JMO acknowledges A/Prof Paul Lockhart and A/Prof Bryony Nayagam for their recent support and commitment as supervisors. Thanks also to Ashwyn Perera and the Animal House Staff at MCRI for their service towards this project.