Associated Papers
Bilateral plaque like macular atrophy and pigmentary retinopathy in an infant with a missense mutation in the MFF gene.
Kılıçarslan O et al.
Ophthalmic Genetics, 2023
Mitochondrial "dysmorphology" in variant classification.
Shamseldin HE et al.
Human Genetics, 2022
Encephalopathy due to defective mitochondrial and peroxisomal fission 2 caused by a novel MFF gene mutation in a young child.
Panda I et al.
Clinical Genetics, 2020
Clinical and Biochemical Features in a Patient With Mitochondrial Fission Factor Gene Alteration.
Nasca A et al.
Frontiers in Genetics, 2018
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