MFF

Publications

Shamseldin HE et al. Genomic analysis of mitochondrial diseases in a consanguineous population reveals novel candidate disease genes. J Med Genet. 2012;49(4):234-41.  PMID: 22499341.

Koch J et al. Disturbed mitochondrial and peroxisomal dynamics due to loss of MFF causes Leigh-like encephalopathy, optic atrophy and peripheral neuropathy. J Med Genet. 2016; 53(4):270-8.  PMID: 26783368.

Nasca A et al. Clinical and Biochemical Features in a Patient With Mitochondrial Fission Factor Gene Alteration. Front Genet. 2018;9:625.  PMID: 30581454.