Respiratory chain complex V deficiency due to a mutation in the assembly gene ATP12

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Respiratory chain complex V deficiency due to a mutation in the assembly gene ATP12.

In patients with mitochondrial encephalomyopathies an increasing number of causative gene defects have been detected. The number of identified pathogenic mitochondrial DNA mutations has largely increased over the past 15 years. Recently, much attention has turned to the investigation of nuclear oxidative phosphorylation (OXPHOS) gene defects. Within the OXPHOS defects, complex V deficiency is r...

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ژورنال

عنوان ژورنال: Journal of Medical Genetics

سال: 2004

ISSN: 1468-6244

DOI: 10.1136/jmg.2003.012047