Order Article Reprints

von Wrede R, Jeub M, Ariöz I, Elger CE, von Voss H, Klein H-G, Becker AJ, Schoch S, Surges R, Kunz WS. Novel KCNH1 Mutations Associated with Epilepsy: Broadening the Phenotypic Spectrum of KCNH1-Associated Diseases. Genes. 2021; 12(2):132. https://doi.org/10.3390/genes12020132

von Wrede, Randi, Monika Jeub, Idil Ariöz, Christian E. Elger, Hubertus von Voss, Hanns-Georg Klein, Albert J. Becker, Susanne Schoch, Rainer Surges, and Wolfram S. Kunz. 2021. "Novel KCNH1 Mutations Associated with Epilepsy: Broadening the Phenotypic Spectrum of KCNH1-Associated Diseases" Genes 12, no. 2: 132. https://doi.org/10.3390/genes12020132

von Wrede, R., Jeub, M., Ariöz, I., Elger, C. E., von Voss, H., Klein, H. -G., Becker, A. J., Schoch, S., Surges, R., & Kunz, W. S. (2021). Novel KCNH1 Mutations Associated with Epilepsy: Broadening the Phenotypic Spectrum of KCNH1-Associated Diseases. Genes, 12(2), 132. https://doi.org/10.3390/genes12020132