A novel, long-lived, and highly engraftable immunodeficient mouse model of mucopolysaccharidosis type I

Author:

Mendez Daniel C,Stover Alexander E,Rangel Anthony D,Brick David J,Nethercott Hubert E,Torres Marissa A,Khalid Omar,Wong Andrew MS,Cooper Jonathan D,Jester James V,Monuki Edwin S,McGuire Cian,Le Steven Q,Kan Shih-hsin,Dickson Patricia I,Schwartz Philip H

Publisher

Elsevier BV

Subject

Genetics,Molecular Biology,Molecular Medicine

Reference42 articles.

1. Molecular genetics of mucopolysaccharidosis type I: diagnostic, clinical, and biological implications;Scott;Hum Mutat,1995

2. Neuropsychological development in children with Hurler syndrome following hematopoietic stem cell transplantation;Peters;Pediatr Transplant,1998

3. The clinical spectrum of alpha-L-iduronidase deficiency;Roubicek;Am J Med Genet,1985

4. Allogeneic stem cell transplantation for the treatment of lysosomal and peroxisomal metabolic diseases;Krivit;Springer Semin Immunopathol,2004

5. Laronidase treatment of mucopolysaccharidosis I;Wraith;BioDrugs,2005

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