F. Oca

Early-onset Behr syndrome due to compound heterozygous mutations in OPA1.

V. Desquiret-Dumas, E. Colin, D. Bonneau, 2014, Brain : a journal of neurology.

Recurrent Isolated Neonatal Hemolytic Anemia: Think About Glutathione Synthetase Deficiency

P. Reynier, G. Simard, F. Oca, 2016, Pediatrics.

Perspectives of drug-based neuroprotection targeting mitochondria.

C. Bris, D. Bonneau, P. Amati‐Bonneau, 2014, Revue neurologique.

Amniotic fluid digestive enzyme analysis is useful for identifying CFTR gene mutations of unclear significance.

B. Gérard, E. Girodon, F. Oca, 2009, Clinical chemistry.

Classification of 101 BRCA1 and BRCA2 variants of uncertain significance by cosegregation study: A powerful approach.

F. Révillion, R. Lidereau, N. Sevenet, 2021, American journal of human genetics.