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Endres D, Decher N, Röhr I, Vowinkel K, Domschke K, Komlosi K, Tzschach A, Gläser B, Schiele MA, Runge K, et al. New Cav1.2 Channelopathy with High-Functioning Autism, Affective Disorder, Severe Dental Enamel Defects, a Short QT Interval, and a Novel CACNA1C Loss-of-Function Mutation. International Journal of Molecular Sciences. 2020; 21(22):8611. https://doi.org/10.3390/ijms21228611

Endres, Dominique, Niels Decher, Isabell Röhr, Kirsty Vowinkel, Katharina Domschke, Katalin Komlosi, Andreas Tzschach, Birgitta Gläser, Miriam A. Schiele, Kimon Runge, and et al. 2020. "New Cav1.2 Channelopathy with High-Functioning Autism, Affective Disorder, Severe Dental Enamel Defects, a Short QT Interval, and a Novel CACNA1C Loss-of-Function Mutation" International Journal of Molecular Sciences 21, no. 22: 8611. https://doi.org/10.3390/ijms21228611

Endres, D., Decher, N., Röhr, I., Vowinkel, K., Domschke, K., Komlosi, K., Tzschach, A., Gläser, B., Schiele, M. A., Runge, K., Süß, P., Schuchardt, F., Nickel, K., Stallmeyer, B., Rinné, S., Schulze-Bahr, E., & Tebartz van Elst, L. (2020). New Cav1.2 Channelopathy with High-Functioning Autism, Affective Disorder, Severe Dental Enamel Defects, a Short QT Interval, and a Novel CACNA1C Loss-of-Function Mutation. International Journal of Molecular Sciences, 21(22), 8611. https://doi.org/10.3390/ijms21228611