I. Lemière

Two new cases of mitochondrial myopathy with exercise intolerance, hyperlactatemia and cardiomyopathy, caused by recessive SLC25A4 mutations.

N. Romero, J. Hogrel, P. Laforêt, 2017, Mitochondrion.

Phenotypic diversity associated with the MT-TV gene m.1644G>A mutation, a matter of quantity.

F. Sedel, I. Nelson, S. Allouche, 2014, Mitochondrion.

Two new cases of mitochondrial myopathy with exercise intolerance, hyperlactatemia and cardiomyopathy, caused by recessive SLC25A4 mutations.

N. Romero, J. Hogrel, P. Laforêt, 2017, Mitochondrion.