ATP6 Homoplasmic Mutations Inhibit and Destabilize the Human F1F0-ATP Synthase without Preventing Enzyme Assembly and Oligomerization
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference41 articles.
1. The mutation at nt 8993 of mitochondrial DNA is a common cause of Leigh's syndrome
2. Mutations in subunit 6 of the F1F0-ATP synthase cause two entirely different diseases
3. Mitochondrial DNA 8993 (NARP) mutation presenting with a heterogeneous phenotype including 'cerebral palsy'.
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