Last Updated: 09/26/2026
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Found 2 publications
Limitations of Multigene Next-Generation Sequencing Panel for "Cerebral Palsy" Phenotype and Other Complex Movement Disorders.
Journal: Pediatric neurology
Published: June 27, 2023
Malate dehydrogenase 2 deficiency is an emerging cause of pediatric epileptic encephalopathy with a recognizable biochemical signature.
Journal: Molecular genetics and metabolism reports
Published: October 17, 2022
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Last Updated: 09/26/2026