Query author contributions in Reactome

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Details on Person Kutsche, Kerstin

Class:Id	Person:9644231
_displayName	Kutsche, Kerstin
_timestamp	2019-04-11 14:24:09
created	[InstanceEdit:9644226] Orlic-Milacic, Marija, 2019-04-11
firstname	Kerstin
initial	K
surname	Kutsche
(author)	[LiteratureReference:9644220] Dysregulation of Rho GTPases in the αPix/Arhgef6 mouse model of X-linked intellectual disability is paralleled by impaired structural and synaptic plasticity and cognitive deficits [LiteratureReference:9660412] Mutation of SHOC2 promotes aberrant protein N-myristoylation and causes Noonan-like syndrome with loose anagen hair [LiteratureReference:9866222] Mutations of the mitochondrial holocytochrome c-type synthase in X-linked dominant microphthalmia with linear skin defects syndrome [LiteratureReference:9941281] Bi-allelic Pathogenic Variants in HS2ST1 Cause a Syndrome Characterized by Developmental Delay and Corpus Callosum, Skeletal, and Renal Abnormalities
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No pathways have been reviewed or authored by Kutsche, Kerstin (9644231)