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Published Erratum
. 2023 Aug 7;15(8):e17911.
doi: 10.15252/emmm.202317911. Epub 2023 Jul 11.

MSTO1 is a cytoplasmic pro-mitochondrial fusion protein, whose mutation induces myopathy and ataxia in humans

Aniko Gal, Peter Balicza, David Weaver, Shamim Naghdi, Suresh K Joseph, Péter Várnai, Tibor Gyuris, Attila Horváth, Laszlo Nagy, Erin L Seifert, Maria Judit Molnar, György Hajnóczky
Published Erratum

MSTO1 is a cytoplasmic pro-mitochondrial fusion protein, whose mutation induces myopathy and ataxia in humans

Aniko Gal et al. EMBO Mol Med. .

Abstract

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Erratum for

References

    1. Gai A, Santos JH, Molnar MJ, Hajnoczky G (2023) Answer to Gerber et al “Autosomal recessive pathogenic MSTO1 variants in hereditary optic atrophy”. EMBO Mol Med 15: e16251 - PMC - PubMed
    1. Gerber S, Lessard L, Rouzier C, Ait-el-Mkadem Saadi S, Ameli R, Thobois S, Abouaf L, Bouhour F, Kaplan J, Putoux A, Pegat A et al (2023) Autosomal recessive pathogenic MSTO1 variants in hereditary optic atrophy. EMBO Mol Med 15: e16090 - PMC - PubMed

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