A shared pattern of altered gene expression in human embryos affected by mitochondrial diseases.
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A. Munnich | N. Frydman | A. Rötig | P. Nitschké | J. Steffann | N. Cagnard | C. Bole | S. Monnot | A. Mayeur | M. Zarhrate | F. Jabot-Hanin | K. Chatzovoulou