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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: https://doi.org/10.1186/s12881-016-0316-0

Published Online: 2016-09-08

Published Print: 2016-12

Update policy: https://doi.org/10.1007/springer_crossmark_policy

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