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Congenital Disorder of Glycosylation Ir
A congenital disorder of glycosylation I that is characterized by failure to thrive, developmental delay, hypotonia, strabismus and hepatic dysfunction and is caused by compound heterozygous mutation in the DDOST gene on
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Overview
A congenital disorder of glycosylation I that is characterized by failure to thrive, developmental delay, hypotonia, strabismus and hepatic dysfunction and is caused by compound heterozygous mutation in the DDOST gene on
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