APA
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. (20200309). Mutations in ELAC2 associated with hypertrophic cardiomyopathy impair mitochondrial tRNA 3'-end processing. : Human mutation.
Chicago
Saoura Makenzie, Powell Christopher A, Kopajtich Robert, Alahmad Ahmad, Al-Balool Haya H, Albash Buthaina, Alfadhel Majid, Alston Charlotte L, Bertini Enrico, Bonnen Penelope E, Bratkovic Drago, Carrozzo Rosalba, Donati Maria A, Di Nottia Michela, Ghezzi Daniele, Goldstein Amy, Haan Eric, Horvath Rita, Hughes Joanne, Invernizzi Federica, Lamantea Eleonora, Lucas Benjamin, Pinnock Kyla-Gaye, Pujantell Maria, Rahman Shamima, Rebelo-Guiomar Pedro, Santra Saikat, Verrigni Daniela, McFarland Robert, Prokisch Holger, Taylor Robert W, Levinger Louis and Minczuk Michal. 20200309. Mutations in ELAC2 associated with hypertrophic cardiomyopathy impair mitochondrial tRNA 3'-end processing. : Human mutation.
Harvard
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. and Minczuk M. (20200309). Mutations in ELAC2 associated with hypertrophic cardiomyopathy impair mitochondrial tRNA 3'-end processing. : Human mutation.
MLA
Saoura Makenzie, Powell Christopher A, Kopajtich Robert, Alahmad Ahmad, Al-Balool Haya H, Albash Buthaina, Alfadhel Majid, Alston Charlotte L, Bertini Enrico, Bonnen Penelope E, Bratkovic Drago, Carrozzo Rosalba, Donati Maria A, Di Nottia Michela, Ghezzi Daniele, Goldstein Amy, Haan Eric, Horvath Rita, Hughes Joanne, Invernizzi Federica, Lamantea Eleonora, Lucas Benjamin, Pinnock Kyla-Gaye, Pujantell Maria, Rahman Shamima, Rebelo-Guiomar Pedro, Santra Saikat, Verrigni Daniela, McFarland Robert, Prokisch Holger, Taylor Robert W, Levinger Louis and Minczuk Michal. Mutations in ELAC2 associated with hypertrophic cardiomyopathy impair mitochondrial tRNA 3'-end processing. : Human mutation. 20200309.