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Congenital Disorder of Glycosylation Ij
A congenital disorder of glycosylation I that is characterized by hypotonia, intractable seizures, developmental delay, microcephaly and severe fetal hypokinesia and is caused by homozygous or compound heterozygous mutat
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Overview
A congenital disorder of glycosylation I that is characterized by hypotonia, intractable seizures, developmental delay, microcephaly and severe fetal hypokinesia and is caused by homozygous or compound heterozygous mutat
Resources
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