Bölükbaşı, E. Y., Afzal, M., Mümtaz, S., Ahmad, N., Malik, S., Tolun, A., "Progressive SCAR14 with Unclear Speech, Developmental Delay, Tremor, and Behavioral Problems Caused by a Homozygous Deletion of the SPTBN2 Pleckstrin Homology Domain", American Journal of Medical Genetics Part A, 173, 9, 2494-2499, 2017.