Query author contributions in Reactome

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Details on Person Leclerc, D

Class:Id	Person:200677
_displayName	Leclerc, D
_timestamp	2007-07-23 20:23:19
created	[InstanceEdit:200727] D'Eustachio, P, 2007-07-23 20:23:04
firstname	D
initial	D
surname	Leclerc
(author)	[LiteratureReference:200732] Human methionine synthase: cDNA cloning and identification of mutations in patients of the cblG complementation group of folate/cobalamin disorders [LiteratureReference:3149477] Molecular basis for methionine synthase reductase deficiency in patients belonging to the cblE complementation group of disorders in folate/cobalamin metabolism [LiteratureReference:3149537] A common variant in methionine synthase reductase combined with low cobalamin (vitamin B12) increases risk for spina bifida [LiteratureReference:3321910] Cloning and mapping of a cDNA for methionine synthase reductase, a flavoprotein defective in patients with homocystinuria [LiteratureReference:3321964] Functionally null mutations in patients with the cblG-variant form of methionine synthase deficiency [LiteratureReference:3325484] Clustering of mutations in the biotin-binding region of holocarboxylase synthetase in biotin-responsive multiple carboxylase deficiency [LiteratureReference:4167532] Mechanism of biotin responsiveness in biotin-responsive multiple carboxylase deficiency [LiteratureReference:5674165] Cloning, expression and chromosomal mapping of human lysosomal sialidase and characterization of mutations in sialidosis
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No pathways have been reviewed or authored by Leclerc, D (200677)