Mutated PET117 causes complex IV deficiency and is associated with neurodevelopmental regression and medulla oblongata lesions

Overview of attention for article published in Human Genetics, April 2017

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PET117

Cited by user Adas2-9939-5190 on 10 Aug 2018

PET117 homolog is a protein that in humans is encoded by the PET117 gene. Localized to mitochondria, this protein is a chaperone protein involved in the assembly of…