Bell, S., Rousseau, J., Peng, H., Aouabed, Z., Priam, P., Theroux, J., . . . Campeau, P. M. (2019). Mutations in ACTL6B Cause Neurodevelopmental Deficits and Epilepsy and Lead to Loss of Dendrites in Human Neurons. Am J Hum Genet.
Stile di citazione ChicagoBell, Scott, et al. "Mutations in ACTL6B Cause Neurodevelopmental Deficits and Epilepsy and Lead to Loss of Dendrites in Human Neurons." Am J Hum Genet 2019.
Citazione MLABell, Scott, et al. "Mutations in ACTL6B Cause Neurodevelopmental Deficits and Epilepsy and Lead to Loss of Dendrites in Human Neurons." Am J Hum Genet 2019.
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