Clinical and molecular features of three patients with congenital disorders of glycosylation type Ih (CDG-Ih) (ALG8 deficiency)

author
created [InstanceEdit:449648] Jassal, B, 2009-12-02
dbId 449635
displayName Clinical and molecular features of three patients with congenital disorders of glycosylation type Ih (CDG-Ih) (ALG8 deficiency)
journal J Med Genet
modified [InstanceEdit:1614742] D'Eustachio, P, 2011-09-29
pages 550-6
pubMedIdentifier 15235028
schemaClass LiteratureReference
title Clinical and molecular features of three patients with congenital disorders of glycosylation type Ih (CDG-Ih) (ALG8 deficiency)
url http://www.ncbi.nlm.nih.gov/pubmed/15235028
volume 41
year 2004
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