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2. Pathological manifestations of Farber disease in a new mouse model. Beckmann N; Kadow S; Schumacher F; Göthert JR; Kesper S; Draeger A; Schulz-Schaeffer WJ; Wang J; Becker JU; Kramer M; Kühn C; Kleuser B; Becker KA; Gulbins E; Carpinteiro A Biol Chem; 2018 Sep; 399(10):1183-1202. PubMed ID: 29908121 [TBL] [Abstract][Full Text] [Related]
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7. Sulfatide and sphingomyelin loading of living cells as tools for the study of ceramide turnover by lysosomal ceramidase--implications for the diagnosis of Farber disease. Levade T; Tempesta MC; Moser HW; Fensom AH; Harzer K; Moser AB; Salvayre R Biochem Mol Med; 1995 Apr; 54(2):117-25. PubMed ID: 8581356 [TBL] [Abstract][Full Text] [Related]
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12. Molecular basis of acid ceramidase deficiency in a neonatal form of Farber disease: identification of the first large deletion in ASAH1 gene. Alves MQ; Le Trionnaire E; Ribeiro I; Carpentier S; Harzer K; Levade T; Ribeiro MG Mol Genet Metab; 2013 Jul; 109(3):276-81. PubMed ID: 23707712 [TBL] [Abstract][Full Text] [Related]
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