APA
Schmelzer L., Smitka M., Wolf C., Lucas N., Tüngler V., Hahn G., Tzschach A., Di Donato N., Lee-Kirsch M. A. & von der Hagen M. (20180702). Variable clinical phenotype in two siblings with Aicardi-Goutières syndrome type 6 and a novel mutation in the ADAR gene. : European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.
Chicago
Schmelzer Lisa, Smitka Martin, Wolf Christine, Lucas Nadja, Tüngler Victoria, Hahn Gabriele, Tzschach Andreas, Di Donato Nataliya, Lee-Kirsch Min Ae and von der Hagen Maja. 20180702. Variable clinical phenotype in two siblings with Aicardi-Goutières syndrome type 6 and a novel mutation in the ADAR gene. : European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.
Harvard
Schmelzer L., Smitka M., Wolf C., Lucas N., Tüngler V., Hahn G., Tzschach A., Di Donato N., Lee-Kirsch M. A. and von der Hagen M. (20180702). Variable clinical phenotype in two siblings with Aicardi-Goutières syndrome type 6 and a novel mutation in the ADAR gene. : European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.
MLA
Schmelzer Lisa, Smitka Martin, Wolf Christine, Lucas Nadja, Tüngler Victoria, Hahn Gabriele, Tzschach Andreas, Di Donato Nataliya, Lee-Kirsch Min Ae and von der Hagen Maja. Variable clinical phenotype in two siblings with Aicardi-Goutières syndrome type 6 and a novel mutation in the ADAR gene. : European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society. 20180702.