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.
Citace podle Chicago (17th ed.)O'Donnell-Luria, A., L. Pais, V. Faundes, X. Lu, J. Taylor, J. Zak, a E. al. Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy. Cell Press, 2019.
Citace podle MLA (9th ed.)O'Donnell-Luria, A., et al. Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy. Cell Press, 2019.
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