Data related to article ": Neonatal developmental and epileptic encephalopathy due to autosomal recessive variants in SLC13A5 gene"

Autosomal recessive pathogenic variants of the SLC13A5 gene are associated with severe neonatal epilepsy, developmental delay, and tooth hypoplasia/hypodontia. We report on 14 additional patients and compare their phenotypic features to previously published patients to identify the clinical hallmarks of this disorder