Query author contributions in Reactome

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Details on Person Nitschk�, Patrick

Class:Id	Person:5617720
_displayName	Nitschk�, Patrick
_timestamp	2014-08-14 19:13:56
created	[InstanceEdit:5617706] Rothfels, Karen, 2014-08-14
firstname	Patrick
initial	P
surname	Nitschk�
(author)	[LiteratureReference:5617722] Defects in the IFT-B component IFT172 cause Jeune and Mainzer-Saldino syndromes in humans [LiteratureReference:6792624] Mutations in human lipoyltransferase gene LIPT1 cause a Leigh disease with secondary deficiency for pyruvate and alpha-ketoglutarate dehydrogenase [LiteratureReference:9686596] Human RTEL1 deficiency causes Hoyeraal-Hreidarsson syndrome with short telomeres and genome instability [LiteratureReference:9856303] ADCK4 mutations promote steroid-resistant nephrotic syndrome through CoQ10 biosynthesis disruption [LiteratureReference:9857614] Biallelic Mutations in LIPT2 Cause a Mitochondrial Lipoylation Defect Associated with Severe Neonatal Encephalopathy
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No pathways have been reviewed or authored by Nitschk�, Patrick (5617720)