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APA Citation
Davey, K. M., Parboosingh, J. S., McLeod, D. R., Chan, A., Casey, R., Ferreira, P., Snyder, F. F., Bridge, P. J., & Bernier, F. P. (2006). mutation of DNAJC19, a human homologue of yeast inner mitochondrial membrane co-chaperones, causes DCMA syndrome, a novel autosomal recessive Barth syndrome-like condition. Journal of medical genetics, 43(5), 385–393. http://access.bl.uk/ark:/81055/vdc_100137790277.0x00003c