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8. A boy with a severe phenotype of succinic semialdehyde dehydrogenase deficiency. Yamakawa Y; Nakazawa T; Ishida A; Saito N; Komatsu M; Matsubara T; Obinata K; Hirose S; Okumura A; Shimizu T Brain Dev; 2012 Feb; 34(2):107-12. PubMed ID: 21612881 [TBL] [Abstract][Full Text] [Related]
9. 'Succinic semialdehyde dehydrogenase deficiency: phenotype evolution in an adolescent patient at 20-year follow-up'. Crutchfield SR; Haas RH; Nyhan WL; Gibson KM Dev Med Child Neurol; 2008 Nov; 50(11):880-1. PubMed ID: 18811705 [No Abstract] [Full Text] [Related]
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12. Novel mutations in two unrelated Italian patients with SSADH deficiency. Balzarini M; Rovelli V; Paci S; Rigoldi M; Sanna G; Pillai S; Asunis M; Parini R; Ciminelli BM; Malaspina P Metab Brain Dis; 2019 Oct; 34(5):1515-1518. PubMed ID: 31267348 [TBL] [Abstract][Full Text] [Related]
13. Head bobbing due to succinic semialdehyde dehydrogenase deficiency. O'Rourke DJ; Ryan S; King MD Neurology; 2010 Jun; 74(24):2025. PubMed ID: 20548048 [No Abstract] [Full Text] [Related]
14. Succinic Semialdehyde Dehydrogenase Deficiency in a Chinese Boy: A Novel ALDH5A1 Mutation With Severe Phenotype. Tay CG; Ariffin H; Yap S; Rahmat K; Sthaneshwar P; Ong LC J Child Neurol; 2015 Jun; 30(7):927-31. PubMed ID: 25122112 [TBL] [Abstract][Full Text] [Related]
15. Mental retardation and hypotonia seen in the knock out mouse for Canavan disease is not due to succinate semialdehyde dehydrogenase deficiency. Surendran S; Ezell EL; Quast MJ; Wei J; Tyring SK; Michals-Matalon K; Matalon R Neurosci Lett; 2004 Mar; 358(1):29-32. PubMed ID: 15016427 [TBL] [Abstract][Full Text] [Related]