APA (7th ed.) Citation

Huber, L. M., Subaşıoğlu, A., Garczarczyk-Asim, D., Valovka, T., Müller, T., Adam, R., & Janecke, A. R. (2025). Pathogenic deep intronic PCSK1 variant causes proprotein convertase 1/3 deficiency in a family: Short report. Clinical genetics, 108(1), . https://doi.org/10.1111/cge.14717

Chicago Style (17th ed.) Citation

Huber, Leah M., Aslı Subaşıoğlu, Dorota Garczarczyk-Asim, Taras Valovka, Thomas Müller, Rüdiger Adam, and Andreas R. Janecke. "Pathogenic Deep Intronic PCSK1 Variant Causes Proprotein Convertase 1/3 Deficiency in a Family: Short Report." Clinical Genetics 108, no. 1 (2025). https://doi.org/10.1111/cge.14717.

MLA (9th ed.) Citation

Huber, Leah M., et al. "Pathogenic Deep Intronic PCSK1 Variant Causes Proprotein Convertase 1/3 Deficiency in a Family: Short Report." Clinical Genetics, vol. 108, no. 1, 2025, https://doi.org/10.1111/cge.14717.