Mendoza-Ferreira, N., Coutelier, M., Janzen, E., Hosseinibarkooie, S., Löhr, H., Schneider, S., . . . Wirth, B. (2018). Biallelic CHP1 mutation causes human autosomal recessive ataxia by impairing NHE1 function. Neurol Genet.
Styl ChicagoMendoza-Ferreira, Natalia, et al. "Biallelic CHP1 Mutation Causes Human Autosomal Recessive Ataxia By Impairing NHE1 Function." Neurol Genet 2018.
Citace podle MLAMendoza-Ferreira, Natalia, et al. "Biallelic CHP1 Mutation Causes Human Autosomal Recessive Ataxia By Impairing NHE1 Function." Neurol Genet 2018.
Upozornění: Tyto citace jsou generovány automaticky. Nemusí být zcela správně podle citačních pravidel..