Bereshneh, Ali H, Andrews, Jonathan C, Eberl, Daniel F, Bademci, Guney, Borja, Nicholas A, Bivona, Stephanie, Chung, Wendy K, Yamamoto, Shinya, Wangler, Michael F, McKee, Shane, Tekin, Mustafa, Bellen, Hugo J, and Kanca, Oguz. De novo variants in CDKL1 and CDKL2 are associated with neurodevelopmental symptoms. Retrieved from https://par.nsf.gov/biblio/10578915. The American Journal of Human Genetics . Web. doi:10.1016/j.ajhg.2025.02.019.

Bereshneh, Ali H, Andrews, Jonathan C, Eberl, Daniel F, Bademci, Guney, Borja, Nicholas A, Bivona, Stephanie, Chung, Wendy K, Yamamoto, Shinya, Wangler, Michael F, McKee, Shane, Tekin, Mustafa, Bellen, Hugo J, & Kanca, Oguz. De novo variants in CDKL1 and CDKL2 are associated with neurodevelopmental symptoms. The American Journal of Human Genetics, (). Retrieved from https://par.nsf.gov/biblio/10578915. https://doi.org/10.1016/j.ajhg.2025.02.019

Bereshneh, Ali H, Andrews, Jonathan C, Eberl, Daniel F, Bademci, Guney, Borja, Nicholas A, Bivona, Stephanie, Chung, Wendy K, Yamamoto, Shinya, Wangler, Michael F, McKee, Shane, Tekin, Mustafa, Bellen, Hugo J, and Kanca, Oguz. "De novo variants in CDKL1 and CDKL2 are associated with neurodevelopmental symptoms". The American Journal of Human Genetics (). Country unknown/Code not available: Elsevier Inc. https://doi.org/10.1016/j.ajhg.2025.02.019. https://par.nsf.gov/biblio/10578915.

@article{osti_10578915,
place = {Country unknown/Code not available}, title = {De novo variants in CDKL1 and CDKL2 are associated with neurodevelopmental symptoms}, url = {https://par.nsf.gov/biblio/10578915}, DOI = {10.1016/j.ajhg.2025.02.019}, abstractNote = {}, journal = {The American Journal of Human Genetics}, publisher = {Elsevier Inc}, author = {Bereshneh, Ali H and Andrews, Jonathan C and Eberl, Daniel F and Bademci, Guney and Borja, Nicholas A and Bivona, Stephanie and Chung, Wendy K and Yamamoto, Shinya and Wangler, Michael F and McKee, Shane and Tekin, Mustafa and Bellen, Hugo J and Kanca, Oguz}, }