APA

Rouzier C., Moore D., Delorme C., Lacas-Gervais S., Ait-El-Mkadem S., Fragaki K., Burté F., Serre V., Bannwarth S., Chaussenot A., Catala M., Yu-Wai-Man P. & Paquis-Flucklinger V. (052017). A novel CISD2 mutation associated with a classical Wolfram syndrome phenotype alters Ca2+ homeostasis and ER-mitochondria interactions. : Human molecular genetics.

Chicago

Rouzier Cécile, Moore David, Delorme Cécile, Lacas-Gervais Sandra, Ait-El-Mkadem Samira, Fragaki Konstantina, Burté Florence, Serre Valérie, Bannwarth Sylvie, Chaussenot Annabelle, Catala Martin, Yu-Wai-Man Patrick and Paquis-Flucklinger Véronique. 052017. A novel CISD2 mutation associated with a classical Wolfram syndrome phenotype alters Ca2+ homeostasis and ER-mitochondria interactions. : Human molecular genetics.

Harvard

Rouzier C., Moore D., Delorme C., Lacas-Gervais S., Ait-El-Mkadem S., Fragaki K., Burté F., Serre V., Bannwarth S., Chaussenot A., Catala M., Yu-Wai-Man P. and Paquis-Flucklinger V. (052017). A novel CISD2 mutation associated with a classical Wolfram syndrome phenotype alters Ca2+ homeostasis and ER-mitochondria interactions. : Human molecular genetics.

MLA

Rouzier Cécile, Moore David, Delorme Cécile, Lacas-Gervais Sandra, Ait-El-Mkadem Samira, Fragaki Konstantina, Burté Florence, Serre Valérie, Bannwarth Sylvie, Chaussenot Annabelle, Catala Martin, Yu-Wai-Man Patrick and Paquis-Flucklinger Véronique. A novel CISD2 mutation associated with a classical Wolfram syndrome phenotype alters Ca2+ homeostasis and ER-mitochondria interactions. : Human molecular genetics. 052017.