O’Donnell-Luria, A. H., Pais, L. S., Faundes, V., Wood, J. C., Sveden, A., Luria, V., . . . Rodan, L. H. (2019). Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy. Am J Hum Genet.
Chicago ZitierstilO’Donnell-Luria, Anne H., et al. "Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy." Am J Hum Genet 2019.
MLA ZitierstilO’Donnell-Luria, Anne H., et al. "Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy." Am J Hum Genet 2019.
Achtung: Diese Zitate sind unter Umständen nicht zu 100% korrekt.