Prenatal onset of mitochondrial disease is associated with sideroflexin 4 deficiency
Author:
Funder
Swedish Research Council
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Molecular Medicine
Reference16 articles.
1. Neurodevelopmental manifestations of mitochondrial disease;Falk;J. Dev. Behav. Pediatr.,2010
2. Ophthalmological findings in children and young adults with genetically verified mitochondrial disease;Grönlund;Br. J. Ophthalmol.,2010
3. Macrocytic anemia and mitochondriopathy resulting from a defect in sideroflexin 4;Hildick-Smith;Am. J. Hum. Genet.,2013
4. Neonatal onset of mitochondrial disorders in 129 patients: clinical and laboratory characteristics and a new approach to diagnosis;Honzik;J. Inherit. Metab. Dis.,2012
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