Case report of homozygous deletion involving the first coding exons of GCNT2 isoforms A and B and part of the upstream region of TFAP2A in congenital cataract
Crossref DOI link:
Update policy: https://doi.org/10.1007/SPRINGER_CROSSMARK_POLICY
Reis, Linda M.
Semina, Elena V.
Funding for this research was provided by:
National Eye Institute (R01EY015518)
unspecified valid from 2016-09-08