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PARL deficiency in mouse causes Complex III defects, coenzyme Q depletion, and Leigh-like syndrome
(2019) PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA. 116(1). p.277-286 -
PINK1 loss-of-function mutations affect mitochondrial complex I activity via NdufA10 ubiquinone uncoupling
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LRRK2 controls an EndoA phosphorylation cycle in synaptic endocytosis
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Parkinson's disease mutations in PINK1 result in decreased Complex I activity and deficient synaptic function