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
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
Mitochondrial Fission Factor Gene Mutation: A Dilemma for Prenatal Diagnosis.
Sharma C et al.
International Journal of Applied & Basic Medical Research, 0
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