Cite

APA Citation

    Saoura, M., Powell, C. A., Kopajtich, R., Alahmad, A., AL‐Balool, H. H., Albash, B., Alfadhel, M., Alston, C. L., Bertini, E., Bonnen, P. E., Bratkovic, D., Carrozzo, R., Donati, M. A., Di Nottia, M., Ghezzi, D., Goldstein, A., Haan, E., Horvath, R., Hughes, J., Invernizzi, F., Lamantea, E., Lucas, B., Pinnock, K., Pujantell, M., Rahman, S., Rebelo‐Guiomar, P., Santra, S., Verrigni, D., McFarland, R., Prokisch, H., Taylor, R. W., Levinger, L., & Minczuk, M. (2019). mutations in ELAC2 associated with hypertrophic cardiomyopathy impair mitochondrial tRNA 3′‐end processing. Human mutation, 40(10), 1731–1748. http://access.bl.uk/ark:/81055/vdc_100127980901.0x000034
  
Back to record