Management of manifesting FOXRED1 carriers is complex

Mol Genet Metab Rep. 2019 Feb 23:19:100463. doi: 10.1016/j.ymgmr.2019.100463. eCollection 2019 Jun.

¹ Krankenanstalt Rudolfstiftung, Messerli Institute, Veterinary University of Vienna, Vienna, Austria.
² University of Tunis El Manar, Genomics Platform, Pasteur Institute of Tunis, Tunisia.

No abstract available

Keywords: Complex-I deficiency; Encephalopathy; Epilepsy; Genotype; Lactic acidosis; Mitochondrial; Phenotype.