Altered properties of mitochondrial ATP-synthase in patients with a T → G mutation in the ATPase 6 (subunit a) gene at position 8993 of mtDNA
Author:
Publisher
Elsevier BV
Subject
Molecular Biology,Molecular Medicine
Reference33 articles.
1. The role of the stalk in the coupling mechanism of F1F0-ATPases
2. Sequence and organization of the human mitochondrial genome
3. Retinitis pigmentosa, ataxia, and mental retardation associated with mitochondrial DNA mutation in an Italian family.
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