Associated Papers
The Role of Impaired Mitochondrial Dynamics in MFN2-Mediated Pathology.
Zaman M et al.
Frontiers in Cell and Developmental Biology, 2022
Natural history of Charcot-Marie-Tooth disease type 2A: a large international multicentre study.
Pipis M et al.
Brain : a Journal of Neurology, 2020
A novel MFN2 mutation causes variable clinical severity in a multi-generational CMT2 family.
Dankwa L et al.
Neuromuscular Disorders : Nmd, 2019
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