Novel missense mutation in the bZIP transcription factor, MAF, associated with congenital cataract, developmental delay, seizures and hearing loss (Aymé-Gripp syndrome)
Crossref DOI link:
Update policy: https://doi.org/10.1007/SPRINGER_CROSSMARK_POLICY
Craig, Jamie E.
Lower, Karen M.
Burdon, Kathryn P.
Funding for this research was provided by:
Channel 7 Children's Research Foundation
National Health and Medical Research Council (NHMRC) of Australia
NHMRC Practitioner Fellowship
NHMRC Senior Research Fellowship.