Query author contributions in Reactome

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Details on Person Lamantea, Eleonora

Class:Id	Person:5696060
_displayName	Lamantea, Eleonora
_timestamp	2015-05-27 10:31:42
created	[InstanceEdit:5696020] Jassal, Bijay, 2015-05-27
firstname	Eleonora
initial	E
surname	Lamantea
(author)	[LiteratureReference:5696063] Lack of the mitochondrial protein acylglycerol kinase causes Sengers syndrome [LiteratureReference:6787376] MTO1 mutations are associated with hypertrophic cardiomyopathy and lactic acidosis and cause respiratory chain deficiency in humans and yeast [LiteratureReference:9815327] SLC25A10 biallelic mutations in intractable epileptic encephalopathy with complex I deficiency [LiteratureReference:9865701] Rewiring of the Human Mitochondrial Interactome during Neuronal Reprogramming Reveals Regulators of the Respirasome and Neurogenesis [LiteratureReference:9914463] RNASEH1 Mutations Impair mtDNA Replication and Cause Adult-Onset Mitochondrial Encephalomyopathy
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No pathways have been reviewed or authored by Lamantea, Eleonora (5696060)