APA (7th ed.) Citation

Burkart, S., Spanjaard, M., Kaufmann, L., Hinderhofer, K., Schaaf, C. P., Ries, M., & Hempel, M. (2025). Phenotypical and genotypical expansion of autosomal-dominant KDM1A-related neurodevelopmental disorder spectrum: A case report. American journal of medical genetics, 197(11), . https://doi.org/10.1002/ajmg.a.64144

Chicago Style (17th ed.) Citation

Burkart, Sebastian, Melanie Spanjaard, Lilian Kaufmann, Katrin Hinderhofer, Christian P. Schaaf, Markus Ries, and Maja Hempel. "Phenotypical and Genotypical Expansion of Autosomal-dominant KDM1A-related Neurodevelopmental Disorder Spectrum: A Case Report." American Journal of Medical Genetics 197, no. 11 (2025). https://doi.org/10.1002/ajmg.a.64144.

MLA (9th ed.) Citation

Burkart, Sebastian, et al. "Phenotypical and Genotypical Expansion of Autosomal-dominant KDM1A-related Neurodevelopmental Disorder Spectrum: A Case Report." American Journal of Medical Genetics, vol. 197, no. 11, 2025, https://doi.org/10.1002/ajmg.a.64144.