Authors: Legros, F Chatzoglou, E Frachon, P de Baulny, HO Laforet, P Jardel, C Godinot, C Lombes, A

Citation: F. Legros et al., Functional characterization of novel mutations in the human cytochrome b gene, EUR J HUM G, 9(7), 2001, pp. 510-518

Authors: Barthelemy, C de Baulny, HO Diaz, J Cheval, MA Frachon, P Romero, N Goutieres, F Fardeau, M Lombes, A

Citation: C. Barthelemy et al., Late-onset mitochondrial DNA depletion: DNA copy number, multiple deletions, and compensation, ANN NEUROL, 49(5), 2001, pp. 607-617

Authors: Laforet, P Ziegler, F Sternberg, D Rouche, A Frachon, P Fardeau, M Eymard, B Lombes, A

Citation: P. Laforet et al., MELAS (A3243G) mutation of mitochondrial DNA: a study of the relationshipsbetween the clinical phenotype in 19 patients and morphological and molecular data., REV NEUROL, 156(12), 2000, pp. 1136-1147

Authors: Bakker, A Barthelemy, C Frachon, P Chateau, D Sternberg, D Mazat, JP Lombes, A

Citation: A. Bakker et al., Functional mitochondrial heterogeneity in heteroplasmic cells carrying themitochondrial DNA mutation associated with the MELAS syndrome (mitochondrial encephalopathy, lactic acidosis, and strokelike episodes), PEDIAT RES, 48(2), 2000, pp. 143-150