Article Versions Notes

Thulasirajah S, Wang X, Sell E, Dávila J, Dyment DA, Kernohan KD. A De Novo Missense Variant in TUBG2 in a Child with Global Developmental Delay, Microcephaly, Refractory Epilepsy and Perisylvian Polymicrogyria. Genes. 2023; 14(1):108. https://doi.org/10.3390/genes14010108

Thulasirajah, Salini, Xueqi Wang, Erick Sell, Jorge Dávila, David A. Dyment, and Kristin D. Kernohan. 2023. "A De Novo Missense Variant in TUBG2 in a Child with Global Developmental Delay, Microcephaly, Refractory Epilepsy and Perisylvian Polymicrogyria" Genes 14, no. 1: 108. https://doi.org/10.3390/genes14010108

Thulasirajah, S., Wang, X., Sell, E., Dávila, J., Dyment, D. A., & Kernohan, K. D. (2023). A De Novo Missense Variant in TUBG2 in a Child with Global Developmental Delay, Microcephaly, Refractory Epilepsy and Perisylvian Polymicrogyria. Genes, 14(1), 108. https://doi.org/10.3390/genes14010108