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

Overview of attention for article published in BMC Medical Genomics, September 2016

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Case report of homozygous deletion involving the first coding exons of GCNT2 isoforms A an... https://t.co/nNVLOTpeV4 #Medical #Genetics

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