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PPA1 Deficiency Causes a Deranged Galactose Metabolism Recognizable in Neonatal Screening. [PDF]

open access: yesMetabolites, 2023
Achleitner MT   +11 more
europepmc   +1 more source

PPA2 deficiency-a rare cause of genetic cardiomyopathy: a case report. [PDF]

open access: yesEur Heart J Case Rep
Khetrapal S   +4 more
europepmc   +1 more source

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