Query author contributions in Reactome

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Details on Person Hennet, T

Class:Id	Person:449291
_displayName	Hennet, T
_timestamp	2009-12-02 11:34:25
created	[InstanceEdit:449318] Jassal, B, 2009-12-02
initial	T
surname	Hennet
(author)	[LiteratureReference:449224] Deficiency of the first mannosylation step in the N-glycosylation pathway causes congenital disorder of glycosylation type Ik [LiteratureReference:449280] CDG-IL: an infant with a novel mutation in the ALG9 gene and additional phenotypic features [LiteratureReference:449289] Human RFT1 deficiency leads to a disorder of N-linked glycosylation [LiteratureReference:449292] Identification and functional analysis of a defect in the human ALG9 gene: definition of congenital disorder of glycosylation type IL [LiteratureReference:449635] Clinical and molecular features of three patients with congenital disorders of glycosylation type Ih (CDG-Ih) (ALG8 deficiency) [LiteratureReference:449643] A mutation in the human ortholog of the Saccharomyces cerevisiae ALG6 gene causes carbohydrate-deficient glycoprotein syndrome type-Ic [LiteratureReference:977005] Molecular cloning of a human UDP-galactose:GlcNAcbeta1,3GalNAc beta1, 3 galactosyltransferase gene encoding an O-linked core3-elongation enzyme [LiteratureReference:977024] Biosynthesis of the linkage region of glycosaminoglycans: cloning and activity of galactosyltransferase II, the sixth member of the beta 1,3-galactosyltransferase family (beta 3GalT6) [LiteratureReference:1889993] A beta-1,3-N-acetylglucosaminyltransferase with poly-N-acetyllactosamine synthase activity is structurally related to beta-1,3-galactosyltransferases [LiteratureReference:1981180] Core glycosylation of collagen is initiated by two beta(1-O)galactosyltransferases
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No pathways have been reviewed or authored by Hennet, T (449291)