Query author contributions in Reactome

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Details on Person Yntema, HG

Class:Id	Person:548689
_displayName	Yntema, HG
_timestamp	2010-03-14 01:20:58
created	[InstanceEdit:548773] D'Eustachio, P, 2010-03-14
firstname	Helger G
initial	HG
surname	Yntema
(author)	[LiteratureReference:548702] FACL4, encoding fatty acid-CoA ligase 4, is mutated in nonspecific X-linked mental retardation [LiteratureReference:5623692] Novel NCC mutants and functional analysis in a new cohort of patients with Gitelman syndrome [LiteratureReference:9618944] Diagnostic exome sequencing in persons with severe intellectual disability [LiteratureReference:9620019] Functional characterization of human RSK4, a new 90-kDa ribosomal S6 kinase, reveals constitutive activation in most cell types [LiteratureReference:9755883] Presence of Genetic Variants Among Young Men With Severe COVID-19 [LiteratureReference:9940356] A SWI/SNF-related autism syndrome caused by de novo mutations in ADNP
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No pathways have been reviewed or authored by Yntema, HG (548689)