A Girl with PRRT2 Mutation Presenting with Benign Familial Infantile Seizures Followed by Autistic Regression
Article in Case Reports in Pediatrics (February 2024)
The most recent citing publications are shown below. View all 14 publications that cite this research output on Dimensions.
A new case of concurrent existence of PRRT2-associated paroxysmal movement disorders with c.649dup variant and 16p11.2 microdeletion syndrome
Article in Brain and Development (April 2022)
Genetic Analysis of Children With Unexplained Developmental Delay and/or Intellectual Disability by Whole-Exome Sequencing
Article in Frontiers in Genetics (November 2021)