Author response: Homozygous YME1L1 mutation causes mitochondriopathy with optic atrophy and mitochondrial network fragmentation

Bianca Hartmann,Timothy Wai,Hao Hu,Thomas MacVicar, Luciana Musante,Björn Fischer-Zirnsak, Werner Stenzel,Ralph Gräf, Lambert van den Heuvel, Hans-Hilger Ropers, Thomas F Wienker,Christoph Hübner,Thomas Langer,Angela M Kaindl

crossref（2016）

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