Citace podle APA

Abdulhag, U. N., Soiferman, D., Schueler-Furman, O., Miller, C., Shaag, A., Elpeleg, O., . . . Saada, A. (2015). Mitochondrial complex IV deficiency, caused by mutated COX6B1, is associated with encephalomyopathy, hydrocephalus and cardiomyopathy. Eur J Hum Genet.

Styl Chicago

Abdulhag, Ulla Najwa, Devorah Soiferman, Ora Schueler-Furman, Chaya Miller, Avraham Shaag, Orly Elpeleg, Simon Edvardson, a Ann Saada. "Mitochondrial Complex IV Deficiency, Caused By Mutated COX6B1, Is Associated With Encephalomyopathy, Hydrocephalus and Cardiomyopathy." Eur J Hum Genet 2015.

Citace podle MLA

Abdulhag, Ulla Najwa, et al. "Mitochondrial Complex IV Deficiency, Caused By Mutated COX6B1, Is Associated With Encephalomyopathy, Hydrocephalus and Cardiomyopathy." Eur J Hum Genet 2015.

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