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Homozygous YME1L1 mutation causes mitochondriopathy with optic atrophy and mitochondrial network fragmentation
scientific journal article
Author/s
author: Hans-Hilger Ropers, Thomas MacVicar, Luciana Musante, Björn Fischer-Zirnsak, Angela Kaindl, Lambert P van den Heuvel
Work details
Publication date
August 6, 2016
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Language
English
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