Identification and functional analysis of a defect in the human ALG9 gene: definition of congenital disorder of glycosylation type IL

author
created [InstanceEdit:449318] Jassal, B, 2009-12-02
dbId 449292
displayName Identification and functional analysis of a defect in the human ALG9 gene: definition of congenital disorder of glycosylation type IL
journal Am J Hum Genet
modified [InstanceEdit:1614742] D'Eustachio, P, 2011-09-29
pages 146-50
pubMedIdentifier 15148656
schemaClass LiteratureReference
title Identification and functional analysis of a defect in the human ALG9 gene: definition of congenital disorder of glycosylation type IL
url http://www.ncbi.nlm.nih.gov/pubmed/15148656
volume 75
year 2004
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