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Q33765243-0CB04F00-E53A-4AB9-A7D0-C49948DA8D77
Q33765243-0CB04F00-E53A-4AB9-A7D0-C49948DA8D77
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http://www.wikidata.org/entity/statement/Q33765243-0CB04F00-E53A-4AB9-A7D0-C49948DA8D77
Deleterious mutation in FDX1L gene is associated with a novel mitochondrial muscle myopathy
P2860
Q33765243-0CB04F00-E53A-4AB9-A7D0-C49948DA8D77
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http://www.wikidata.org/entity/statement/Q33765243-0CB04F00-E53A-4AB9-A7D0-C49948DA8D77
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wasDerivedFrom
c958fb5b8fe29c7b78d0d525cfa9c3bd1232e7ea
P2860
Tissue-specific splicing of ISCU results in a skeletal muscle phenotype in myopathy with lactic acidosis, while complete loss of ISCU results in early embryonic death in mice.