Cita APA (7th ed.)

O'Donnell-Luria, A., Pais, L., Faundes, V., Lu, X., Taylor, J., Zak, J., & al., E. (2019). Heterozygous variants in KMT2E cause a spectrum of neurodevelopmental disorders and epilepsy. Cell Press.

Cita Chicago (17th ed.)

O'Donnell-Luria, A., L. Pais, V. Faundes, X. Lu, J. Taylor, J. Zak, i E. al. Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy. Cell Press, 2019.

Cita MLA (9th ed.)

O'Donnell-Luria, A., et al. Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy. Cell Press, 2019.