Bénédicte Mousson de Camaret

Prevalence of rare mitochondrial DNA mutations in mitochondrial disorders

Sylvie Bannwarth, Vincent Procaccio, Anne Sophie Lebre et al. · Journal of Medical Genetics · 2013 · 189 citations · Full text

Structural organization of mitochondrial human complex I: role of the ND4 and ND5 mitochondria-encoded subunits and interaction with prohibitin

Ingrid Bourges, Claire Ramus, Bénédicte Mousson de Camaret et al. · Biochemical Journal · 2004 · 133 citations · Full text

Complete loss of expression of the <i>ANT1</i> gene causing cardiomyopathy and myopathy

Andoni Echaniz‐Laguna, Maïté Chassagne, Jennifer Ceresuela et al. · Journal of Medical Genetics · 2011 · 72 citations

SURF1 deficiency causes demyelinating Charcot-Marie-Tooth disease

Andoni Echaniz‐Laguna, Daniele Ghezzi, Maïté Chassagne et al. · Neurology · 2013 · 64 citations · Full text

Quantification of Mitochondrial DNA Deletion, Depletion, and Overreplication: Application to Diagnosis

Béatrice Chabi, Bénédicte Mousson de Camaret, Hervé Duborjal et al. · Clinical Chemistry · 2003 · 63 citations · Full text