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Clinical and Molecular Characteristics of Neuronal Ceroid Lipofuscinosis in Saudi Arabia.
Saleh MM, Hamhom AM, Al-Otaibi A, AlGhamdi M, Housawi Y, Aljadhai YI, Alameer S, Almannai M, Jad LA, Alwadei AH, Tabassum S, Alsaman A, AlAsmari A, Al Mutairi F, Althiyab H, Bashiri FA, AlHumaidi S, Alfadhel M, Mink JW, AlHashim A, Faqeih EA; Saudi NCL Study Consortium. Saleh MM, et al. Pediatr Neurol. 2024 Mar 7;155:149-155. doi: 10.1016/j.pediatrneurol.2024.03.004. Online ahead of print. Pediatr Neurol. 2024. PMID: 38653183
The First Reported Case of a Child with Two Different Rare Metabolic Disorders: Very Long-Chain Acyl-CoA Dehydrogenase Deficiency and Encephalomyopathic Mitochondrial DNA Depletion Syndrome 13.
Alotaibi M, Alqasmi A, Albassam F, Alkahtani T, Alqahtany M, Alkhaldi M. Alotaibi M, et al. Among authors: albassam f. Glob Med Genet. 2023 Oct 10;10(4):278-281. doi: 10.1055/s-0043-1775979. eCollection 2023 Dec. Glob Med Genet. 2023. PMID: 37822418 Free PMC article.