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marino iskandar[Author]
(3 results)?
Limitations of Multigene Next-Generation Sequencing Panel for "Cerebral Palsy" Phenotype and Other Complex Movement Disorders.
Pediatr Neurol. 2023 Dec;149:15-18. doi: 10.1016/j.pediatrneurol.2023.08.040. Epub 2023 Sep 2.
Pediatr Neurol. 2023.
PMID: 37757660
Malate dehydrogenase 2 deficiency is an emerging cause of pediatric epileptic encephalopathy with a recognizable biochemical signature.
Priestley JRC, Pace LM, Sen K, Aggarwal A, Alves CAPF, Campbell IM, Cuddapah SR, Engelhardt NM, Eskandar M, Jolín García PC, Gropman A, Helbig I, Hong X, Gowda VK, Lusk L, Trapane P, Srinivasan VM, Suwannarat P, Ganetzky RD.
Priestley JRC, et al. Among authors: eskandar m.
Mol Genet Metab Rep. 2022 Nov 16;33:100931. doi: 10.1016/j.ymgmr.2022.100931. eCollection 2022 Dec.
Mol Genet Metab Rep. 2022.
PMID: 36420423
Free PMC article.
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