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Dive into the research topics of 'Mitochondrial myopathy and complex III deficiency in a patient with a new stop-codon mutation (G339X) in the cytochrome b gene'. Together they form a unique fingerprint.- Sort by
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Michelangelo Mancuso, Massimiliano Filosto, J. Clarke Stevens, Marc Patterson, Sara Shanske, Sindu Krishna, Salvatore DiMauro
Research output: Contribution to journal › Article › peer-review