Bordoni, Andreina

Mutations of mitochondrial DNA polymerase γA are a frequent cause of autosomal dominant or recessive progressive external ophthalmoplegia

Lamantea, E., Tiranti, V., Bordoni, A., Toscano, A., Bono, F., Servidei, S., Papadimitriou, A., Spelbrink, H., Silvestri, L., Casari, G., et al. (2002) · Annals of Neurology

Mitochondrial Function and PathologyHereditary Neurological Disorders

Cited by 270

The Mitochondrial Disulfide Relay System Protein GFER Is Mutated in Autosomal-Recessive Myopathy with Cataract and Combined Respiratory-Chain Deficiency

Di Fonzo, A., Ronchi, D., Lodi, T., Fassone, E., Tigano, M., Lamperti, C., Corti, S., Bordoni, A., Fortunato, F., Nizzardo, M., et al. (2009) · The American Journal of Human Genetics

Mitochondrial Function and PathologyMetabolism and Genetic Disorders

Cited by 141

Skeletal muscle gene expression profiling in mitochondrial disorders

Crimi, M., Bordoni, A., Menozzi, G., Riva, L., Fortunate, F., Galbiati, S., Del Bo, R., Pozzoli, U., Bresolin, N., & Comi, G. P. (2005) · The FASEB Journal

Mitochondrial Function and PathologyMuscle Physiology and Disorders

Cited by 56