Reactome | Delahodde, A

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created	[InstanceEdit:6792635] Jassal, Bijay, 2015-08-25
dbId	6792628
displayName	Delahodde, A
firstname	Agn�s
initial	A
publications	[LiteratureReference:6792624] Mutations in human lipoyltransferase gene LIPT1 cause a Leigh disease with secondary deficiency for pyruvate and alpha-ketoglutarate dehydrogenase [LiteratureReference:9857614] Biallelic Mutations in LIPT2 Cause a Mitochondrial Lipoylation Defect Associated with Severe Neonatal Encephalopathy
schemaClass	Person
surname	Delahodde

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