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congenital disorder of glycosylation type 1H
Also see congenital disorder of glycosylation
Genetics:
- associated with mutation in gene for ALG8
Related
dolichyl pyrophosphate Glc1man9GlcNAc2 alpha-1,3-glucosyltransferase; asparagine-linked glycosylation protein 8 homolog; dol-P-Glc:Glc(1)man(9)GlcNAc(2)-PP-dolichyl alpha-1,3-glucosyltransferase; dolichyl-P-Glc:Glc1man9GlcNAc2-PP-dolichyl glucosyltransferase (ALG8, HUSSY-2)
General
congenital disorder of glycosylation
Database Correlations
OMIM 608104
References
OMIM :accession 608104