APA
Heimer G., Kerätär J. M., Riley L. G., Balasubramaniam S., Eyal E., Pietikäinen L. P., Hiltunen J. K., Marek-Yagel D., Hamada J., Gregory A., Rogers C., Hogarth P., Nance M. A., Shalva N., Veber A., Tzadok M., Nissenkorn A., Tonduti D., Renaldo F., Kraoua I., Panteghini C., Valletta L., Garavaglia B., Cowley M. J., Gayevskiy V., Roscioli T., Silberstein J. M., Hoffmann C., Raas-Rothschild A., Tiranti V., Anikster Y., Christodoulou J., Kastaniotis A. J., Ben-Zeev B. & Hayflick S. J. (20170523). MECR Mutations Cause Childhood-Onset Dystonia and Optic Atrophy, a Mitochondrial Fatty Acid Synthesis Disorder. : American journal of human genetics.
Chicago
Heimer Gali, Kerätär Juha M, Riley Lisa G, Balasubramaniam Shanti, Eyal Eran, Pietikäinen Laura P, Hiltunen J Kalervo, Marek-Yagel Dina, Hamada Jeffrey, Gregory Allison, Rogers Caleb, Hogarth Penelope, Nance Martha A, Shalva Nechama, Veber Alvit, Tzadok Michal, Nissenkorn Andreea, Tonduti Davide, Renaldo Florence, Kraoua Ichraf, Panteghini Celeste, Valletta Lorella, Garavaglia Barbara, Cowley Mark J, Gayevskiy Velimir, Roscioli Tony, Silberstein Jonathon M, Hoffmann Chen, Raas-Rothschild Annick, Tiranti Valeria, Anikster Yair, Christodoulou John, Kastaniotis Alexander J, Ben-Zeev Bruria and Hayflick Susan J. 20170523. MECR Mutations Cause Childhood-Onset Dystonia and Optic Atrophy, a Mitochondrial Fatty Acid Synthesis Disorder. : American journal of human genetics.
Harvard
Heimer G., Kerätär J. M., Riley L. G., Balasubramaniam S., Eyal E., Pietikäinen L. P., Hiltunen J. K., Marek-Yagel D., Hamada J., Gregory A., Rogers C., Hogarth P., Nance M. A., Shalva N., Veber A., Tzadok M., Nissenkorn A., Tonduti D., Renaldo F., Kraoua I., Panteghini C., Valletta L., Garavaglia B., Cowley M. J., Gayevskiy V., Roscioli T., Silberstein J. M., Hoffmann C., Raas-Rothschild A., Tiranti V., Anikster Y., Christodoulou J., Kastaniotis A. J., Ben-Zeev B. and Hayflick S. J. (20170523). MECR Mutations Cause Childhood-Onset Dystonia and Optic Atrophy, a Mitochondrial Fatty Acid Synthesis Disorder. : American journal of human genetics.
MLA
Heimer Gali, Kerätär Juha M, Riley Lisa G, Balasubramaniam Shanti, Eyal Eran, Pietikäinen Laura P, Hiltunen J Kalervo, Marek-Yagel Dina, Hamada Jeffrey, Gregory Allison, Rogers Caleb, Hogarth Penelope, Nance Martha A, Shalva Nechama, Veber Alvit, Tzadok Michal, Nissenkorn Andreea, Tonduti Davide, Renaldo Florence, Kraoua Ichraf, Panteghini Celeste, Valletta Lorella, Garavaglia Barbara, Cowley Mark J, Gayevskiy Velimir, Roscioli Tony, Silberstein Jonathon M, Hoffmann Chen, Raas-Rothschild Annick, Tiranti Valeria, Anikster Yair, Christodoulou John, Kastaniotis Alexander J, Ben-Zeev Bruria and Hayflick Susan J. MECR Mutations Cause Childhood-Onset Dystonia and Optic Atrophy, a Mitochondrial Fatty Acid Synthesis Disorder. : American journal of human genetics. 20170523.