M. Monfort

发表

Importance of searching for associated mitochondrial DNA alterations in patients with multiple deletions

C. Richelme, J. Pouget, C. Desnuelle, 2000, European Journal of Human Genetics.

Diagnostic evaluation of clinically normal subjects with chronic hyperCKemia

D. Figarella-Branger, J. Pouget, M. Krahn, 2006, Neurology.

Early-onset fatal encephalomyopathy associated with severe mtDNA depletion

C. Desnuelle, B. Chabrol, J. Camboulives, 1995, European Journal of Pediatrics.