Query author contributions in Reactome

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Details on Person Lichtner, P

Class:Id	Person:70754
_displayName	Lichtner, P
_timestamp	0000-00-00 00:00:00
firstname	Peter
initial	P
surname	Lichtner
(author)	[LiteratureReference:70749] Cloning of the human MCCA and MCCB genes and mutations therein reveal the molecular cause of 3-methylcrotonyl-CoA: carboxylase deficiency [LiteratureReference:1252031] Genetic and structural characterization of the human mitochondrial inner membrane translocase [LiteratureReference:5651949] Hereditary hypophosphatemic rickets with hypercalciuria is caused by mutations in the sodium-phosphate cotransporter gene SLC34A3 [LiteratureReference:9714618] Mutations in RHOT1 Disrupt Endoplasmic Reticulum-Mitochondria Contact Sites Interfering with Calcium Homeostasis and Mitochondrial Dynamics in Parkinson's Disease [LiteratureReference:9828895] Haploinsufficiency of TBK1 causes familial ALS and fronto-temporal dementia
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No pathways have been reviewed or authored by Lichtner, P (70754)