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APA Citation
Marchet, S., Legati, A., Nasca, A., Di Meo, I., Spagnolo, M., Zanetti, N., Lamantea, E., Catania, A., Lamperti, C., & Ghezzi, D. (2020). homozygous mutations in C1QBP as cause of progressive external ophthalmoplegia (PEO) and mitochondrial myopathy with multiple mtDNA deletions. Human mutation, 41(10), 1745–1750. http://access.bl.uk/ark:/81055/vdc_100110783265.0x00002d