Parenti, I., Lehalle, D., Nava, C., Torti, E., Leitão, E., Person, R., . . . Mignot, C. (2021). Missense and truncating variants in CHD5 in a dominant neurodevelopmental disorder with intellectual disability, behavioral disturbances, and epilepsy. Hum Genet.
Citação norma ChicagoParenti, Ilaria, et al. "Missense and Truncating Variants in CHD5 in a Dominant Neurodevelopmental Disorder With Intellectual Disability, Behavioral Disturbances, and Epilepsy." Hum Genet 2021.
MLA CitationParenti, Ilaria, et al. "Missense and Truncating Variants in CHD5 in a Dominant Neurodevelopmental Disorder With Intellectual Disability, Behavioral Disturbances, and Epilepsy." Hum Genet 2021.
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