HORNIG, Tobias, GRÜNING, Björn, KUNDU, Kousik, HOUWAART, Torsten, BACKOFEN, Rolf, BIBER, Knut und NORMANN, Claus, 2019. GRIN3 B missense mutation as an inherited risk factor for schizophrenia: whole-exome sequencing in a family with a familiar history of psychotic disorders. Freiburg: Universität.
Elsevier - Harvard (with titles)Hornig, T., Grüning, B., Kundu, K., Houwaart, T., Backofen, R., Biber, K., Normann, C., 2019. GRIN3 B missense mutation as an inherited risk factor for schizophrenia: whole-exome sequencing in a family with a familiar history of psychotic disorders. Universität, Freiburg. https://doi.org/10.1017/s0016672316000148
American Psychological Association 7th editionHornig, T., Grüning, B., Kundu, K., Houwaart, T., Backofen, R., Biber, K., & Normann, C. (ca. 2019). GRIN3 B missense mutation as an inherited risk factor for schizophrenia: whole-exome sequencing in a family with a familiar history of psychotic disorders [Cd]. Universität. https://doi.org/10.1017/s0016672316000148
Springer - Basic (author-date)Hornig T, Grüning B, Kundu K, Houwaart T, Backofen R, Biber K, Normann C (2019) GRIN3 B missense mutation as an inherited risk factor for schizophrenia: whole-exome sequencing in a family with a familiar history of psychotic disorders. Universität, Freiburg
Juristische Zitierweise (Stüber) (Deutsch)Hornig, Tobias/ Grüning, Björn/ Kundu, Kousik/ Houwaart, Torsten/ Backofen, Rolf/ Biber, Knut/ Normann, Claus, GRIN3 B missense mutation as an inherited risk factor for schizophrenia: whole-exome sequencing in a family with a familiar history of psychotic disorders, Freiburg 2019.