Language
English
Publication Date
9-1-2023
Journal
European Journal of Human Genetics
DOI
10.1038/s41431-023-01348-2
PMID
37029317
PMCID
PMC10474260
PubMedCentral® Posted Date
4-7-2023
PubMedCentral® Full Text Version
Post-print
Keywords
Humans, Homozygote, Genotype, Neurodevelopmental Disorders, Heterozygote, Epilepsy
Published Open-Access
yes
Recommended Citation
Esmeralda Villavicencio Gonzalez and Ryan S Dhindsa, "Studying Ultra-Rare Variants in STX1A Uncovers a Novel Neurodevelopmental Disorder" (2023). Faculty, Staff and Students Publications. 6235.
https://digitalcommons.library.tmc.edu/baylor_docs/6235