REIFF, Charlotte M., OWCZAREK-LIPSKA, Marta, SPITAL, Georg Ulrich Johannes, RÖGER, Carsten, HINZ, Hebke, JÜSCHKE, Christoph, THIELE, Holger, ALTMÜLLER, Janine, NÜRNBERG, Peter, DA COSTA, Romain Vivien und NEIDHARDT, John, 2025. The mutation p.E113 K in the Schiff base counterion of rhodopsin is associated with two distinct retinal phenotypes within the same family. Freiburg: Universität.
Elsevier - Harvard (with titles)Reiff, C.M., Owczarek-Lipska, M., Spital, G.U.J., Röger, C., Hinz, H., Jüschke, C., Thiele, H., Altmüller, J., Nürnberg, P., Da Costa, R.V., Neidhardt, J., 2025. The mutation p.E113 K in the Schiff base counterion of rhodopsin is associated with two distinct retinal phenotypes within the same family. Universität, Freiburg. https://doi.org/10.1038/srep36208
American Psychological Association 7th editionReiff, C. M., Owczarek-Lipska, M., Spital, G. U. J., Röger, C., Hinz, H., Jüschke, C., Thiele, H., Altmüller, J., Nürnberg, P., Da Costa, R. V., & Neidhardt, J. (ca. 2025). The mutation p.E113 K in the Schiff base counterion of rhodopsin is associated with two distinct retinal phenotypes within the same family [Cd]. Universität. https://doi.org/10.1038/srep36208
Springer - Basic (author-date)Reiff CM, Owczarek-Lipska M, Spital GUJ, Röger C, Hinz H, Jüschke C, Thiele H, Altmüller J, Nürnberg P, Da Costa RV, Neidhardt J (2025) The mutation p.E113 K in the Schiff base counterion of rhodopsin is associated with two distinct retinal phenotypes within the same family. Universität, Freiburg
Juristische Zitierweise (Stüber) (Deutsch)Reiff, Charlotte M./ Owczarek-Lipska, Marta/ Spital, Georg Ulrich Johannes/ Röger, Carsten/ Hinz, Hebke/ Jüschke, Christoph/ Thiele, Holger/ Altmüller, Janine/ Nürnberg, Peter/ Da Costa, Romain Vivien/ Neidhardt, John, The mutation p.E113 K in the Schiff base counterion of rhodopsin is associated with two distinct retinal phenotypes within the same family, Freiburg 2025.