Hélène Pagniez-Mammeri

Mitochondrial complex I deficiency of nuclear origin I. Structural genes.

P. Bénit, P. Rustin, A. Legrand, 2012, Molecular genetics and metabolism.

Leukoencephalopathy with vanishing white matter caused by compound heterozygous mutations in mitochondrial complex I NDUFS1 subunit.

A. Legrand, P. Landrieu, A. Slama, 2010, Molecular genetics and metabolism.

Rapid screening for nuclear genes mutations in isolated respiratory chain complex I defects.

A. Legrand, P. Landrieu, A. Slama, 2009, Molecular genetics and metabolism.

Mitochondrial complex I deficiency of nuclear origin II. Non-structural genes.

P. Bénit, P. Rustin, Malgorzata Rak, 2012, Molecular genetics and metabolism.