Query author contributions in Reactome

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Details on Person Kuss, Andreas W

Class:Id	Person:3702103
_displayName	Kuss, Andreas W
_timestamp	2013-06-13 12:04:19
created	[InstanceEdit:3702106] Jassal, B, 2013-06-13
firstname	Andreas W
initial	AW
surname	Kuss
(author)	[LiteratureReference:3702124] Homozygosity mapping in consanguineous families reveals extreme heterogeneity of non-syndromic autosomal recessive mental retardation and identifies 8 novel gene loci [LiteratureReference:3702132] ST3GAL3 mutations impair the development of higher cognitive functions [LiteratureReference:3702145] West syndrome caused by ST3Gal-III deficiency [LiteratureReference:4420042] Next generation sequencing in a family with autosomal recessive Kahrizi syndrome (OMIM 612713) reveals a homozygous frameshift mutation in SRD5A3 [LiteratureReference:4839778] Mutations in the alpha 1,2-mannosidase gene, MAN1B1, cause autosomal-recessive intellectual disability [LiteratureReference:8955442] CCDC22 deficiency in humans blunts activation of proinflammatory NF-κB signaling
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No pathways have been reviewed or authored by Kuss, Andreas W (3702103)