Query author contributions in Reactome

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Details on Person Raas-Rothschild, Annick

Class:Id	Person:2485044
_displayName	Raas-Rothschild, Annick
_timestamp	2012-09-27 17:27:36
created	[InstanceEdit:2485050] Orlic-Milacic, M, 2012-09-27
firstname	Annick
initial	A
surname	Raas-Rothschild
(author)	[LiteratureReference:2485042] The molecular mechanism underlying Roberts syndrome involves loss of ESCO2 acetyltransferase activity [LiteratureReference:5229105] Adaptor protein complex 4 deficiency causes severe autosomal-recessive intellectual disability, progressive spastic paraplegia, shy character, and short stature [LiteratureReference:8853703] Angiokeratoma corporis diffusum in human beta-mannosidosis: Report of a new case and a novel mutation [LiteratureReference:8875837] Impaired mitochondrial glutamate transport in autosomal recessive neonatal myoclonic epilepsy [LiteratureReference:9823180] Characterization of SETD1A haploinsufficiency in humans and Drosophila defines a novel neurodevelopmental syndrome
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No pathways have been reviewed or authored by Raas-Rothschild, Annick (2485044)