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EJHG.2013.269
EJHG.2013.269
http://dx.doi.org/10.1038/EJHG.2013.269
Deleterious mutation in FDX1L gene is associated with a novel mitochondrial muscle myopathy
P356
Q33765243-5EBE0114-5AB9-4C42-88FF-FA066C62CCB9
P356
EJHG.2013.269
http://dx.doi.org/10.1038/EJHG.2013.269