APA aipamena

Barcia, G., Assouline, Z., Pennisi, A., Gitiaux, C., Schiff, M., Boddaert, N., . . . Rötig, A. (2019). Cytochrome c oxidase deficiency caused by biallelic SCO2 mutations in two sibs with cerebellar ataxia and progressive peripheral axonal neuropathy. Mol Genet Metab Rep.

Chicago Style aipamena

Barcia, Giulia, Zahra Assouline, Alessandra Pennisi, Cyril Gitiaux, Manuel Schiff, Nathalie Boddaert, Arnold Munnich, Jean-Paul Bonnefont, and Agnès Rötig. "Cytochrome C Oxidase Deficiency Caused By Biallelic SCO2 Mutations in Two Sibs With Cerebellar Ataxia and Progressive Peripheral Axonal Neuropathy." Mol Genet Metab Rep 2019.

MLA aipamena

Barcia, Giulia, et al. "Cytochrome C Oxidase Deficiency Caused By Biallelic SCO2 Mutations in Two Sibs With Cerebellar Ataxia and Progressive Peripheral Axonal Neuropathy." Mol Genet Metab Rep 2019.

Kontuz: berrikusi erreferentzia hauek erabili aurretik.