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Details on Person Clinical and genetic spectrum of pyruvate dehydrogenase deficiency: dihydrolipoamide acetyltransferase (E2) deficiency

Class:IdLiteratureReference:450841
_displayNameClinical and genetic spectrum of pyruvate dehydrogenase deficiency: dihydrolipoamide acetyltransferase (E2) deficiency
_timestamp2009-12-17 23:34:11
author[Person:70068] Head, RA
[Person:70067] Brown, RM
[Person:450843] Zolkipli, Z
[Person:450849] Shahdadpuri, R
[Person:450852] King, MD
[Person:193462] Clayton, Peter T
[Person:70069] Brown, GK
created[InstanceEdit:450853] D'Eustachio, P, 2009-12-17
journalAnn Neurol
pages234-41
pubMedIdentifier16049940
titleClinical and genetic spectrum of pyruvate dehydrogenase deficiency: dihydrolipoamide acetyltransferase (E2) deficiency
volume58
year2005
(literatureReference)[Pathway:9861559] PDH complex synthesizes acetyl-CoA from PYR [Homo sapiens]
[Reaction:9861667] DLAT trimer transfers acetyl to CoA [Homo sapiens]
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