Author:
Richard M,Arfi A,Seguin J,Gandolphe C,Scherman D
Publisher
Springer Science and Business Media LLC
Subject
Genetics,Molecular Biology,Molecular Medicine
Reference51 articles.
1. Neufeld EF, Muenzer J . The mucopolysaccharidosis. In: Scriver CR, Beaudet AL, Sly WS, Valle D (eds). Metabol Mol Bases Inherit Dis. MacGraw-Hill: New York, 2001, pp 3421–3452.
2. Birkenmeier EH, Davisson MT, Beamer WG, Ganschow RE, Vogler CA, Gwynn B et al. Murine mucopolysaccharidosis type VII. Characterization of a mouse with beta-glucuronidase deficiency. J Clin Invest 1989; 83: 1258–1266.
3. Vogler C, Barker J, Sands MS, Levy B, Galvin N, Sly WS et al. Murine mucopolysaccharidosis VII: impact of therapies on the phenotype, clinical course, and pathology in a model of a lysosomal storage disease. Pediatr Dev Pathol 2001; 4: 421–433.
4. Vogler C, Levy B, Galvin N, Lessard M, Soper B, Barker J et al. Early onset of lysosomal storage disease in a murine model of mucopolysaccharidosis type VII: undegraded substrate accumulates in many tissues in the fetus and very young MPS VII mouse. Pediatr Dev Pathol 2005; 8: 453–462.
5. Neufeld EF . Lysosomal storage diseases. Annu Rev Biochem 1991; 60: 257–280.
Cited by
23 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献