APA (7th ed.) Citation

Mütze, U., Bürger, F., Hoffmann, J., Tegetmeyer, H., Heichel, J., Nickel, P., . . . Beblo, S. (2017). Multigene panel next generation sequencing in a patient with cherry red macular spot: Identification of two novel mutations in NEU1 gene causing sialidosis type I associated with mild to unspecific biochemical and enzymatic findings. Molecular genetics and metabolism reports, 10, . https://doi.org/10.1016/j.ymgmr.2016.11.004

Chicago Style (17th ed.) Citation

Mütze, Ulrike, Friederike Bürger, Jessica Hoffmann, Helmut Tegetmeyer, Jens Heichel, Petra Nickel, Johannes Lemke, Steffen Syrbe, and Skadi Beblo. "Multigene Panel Next Generation Sequencing in a Patient with Cherry Red Macular Spot: Identification of Two Novel Mutations in NEU1 Gene Causing Sialidosis Type I Associated with Mild to Unspecific Biochemical and Enzymatic Findings." Molecular Genetics and Metabolism Reports 10 (2017). https://doi.org/10.1016/j.ymgmr.2016.11.004.

MLA (9th ed.) Citation

Mütze, Ulrike, et al. "Multigene Panel Next Generation Sequencing in a Patient with Cherry Red Macular Spot: Identification of Two Novel Mutations in NEU1 Gene Causing Sialidosis Type I Associated with Mild to Unspecific Biochemical and Enzymatic Findings." Molecular Genetics and Metabolism Reports, vol. 10, 2017, https://doi.org/10.1016/j.ymgmr.2016.11.004.