Concepedia

Adenine nucleotide translocase is involved in a mitochondrial coupling defect in MFN2-related Charcot–Marie–Tooth type 2A disease

Virginie Guillet, Naïg Guéguen, Christophe Verny, Marc Ferré, Chadi Homedan, Dominique Loiseau, Vincent Procaccio, Patrizia Amati‐Bonneau, Dominique Bonneau, Pascal Reynier,

Neurogenetics · 2009 · 36 citations · 25 references

DOI

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References

25

Mitofusins Mfn1 and Mfn2 coordinately regulate mitochondrial fusion and are essential for embryonic development

Hsiuchen Chen, Scott A. Detmer, Andrew J. Ewald et al. · The Journal of Cell Biology · 2003 · 2.6K citations · Full text

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Mitofusin 2 tethers endoplasmic reticulum to mitochondria

Olga Martins de Brito, Luca Scorrano · Nature · 2008 · 2.4K citations

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Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A

Stephan Züchner, Irina Mersiyanova, M. Muglia et al. · Nature Genetics · 2004 · 1.6K citations · Full text

, , +11

Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophy

Cécile Delettre, Guy Lenaers, Jean‐Michel Griffoin et al. · Nature Genetics · 2000 · 1.4K citations

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OPA1 requires mitofusin 1 to promote mitochondrial fusion

Sara Cipolat, Olga Martins de Brito, Barbara Dal Zilio et al. · Proceedings of the National Academy of Sciences · 2004 · 1.3K citations · Full text

, , +16