Showing results 1 to 2 of 2
Title | Author(s) | Issue Date | |
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Folinic acid responsive epilepsy in Ohtahara Syndrome caused by STXBP1 mutation Journal:Pediatric Neurology | 2014 | ||
Whole Genome Sequencing In Pediatric Channelopathy And Cardiomyopathy Journal:Heart Rhythm | 1-May-2023 |