Gräf, Ralph

University of Potsdam

1 paper on CoChatORCID 0000-0001-5144-868X

Most cited papers

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Homozygous YME1L1 mutation causes mitochondriopathy with optic atrophy and mitochondrial network fragmentation
Hartmann, B., Wai, T., Hu, H., MacVicar, T., Musante, L., Fischer-Zirnsak, B., Stenzel, W., Gräf, R., van den Heuvel, L., Ropers, H.-H., et al. (2016) · eLife
Mitochondrial Function and PathologyAutophagy in Disease and Therapy
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