Characterization of an MPS I-H knock-in mouse that carries a nonsense mutation analogous to the human IDUA-W402X mutation

Author:

Wang Dan,Shukla Charu,Liu Xiaoli,Schoeb Trenton R.,Clarke Lorne A.,Bedwell David M.,Keeling Kim M.

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference53 articles.

1. Pathogenic cascades in lysosomal disease – Why so complex?;Walkley;J. Inherit. Metab. Dis.,2009

2. E.F. Neufeld, J. Muenzer, The Mucopolysaccharidoses, The Online Metabolic & Molecular Bases of Inherited Disease (www.ommbid.com), The McGraw-Hill Companies, 2001, pp. 3421–3452.

3. The cell biology of lysosomal storage disorders;Futerman;Nat. Rev. Mol. Cell Biol.,2004

4. Lysosomal disorders: from storage to cellular damage;Ballabio;Biochim. Biophys. Acta,2009

5. Identification and characterization of the molecular lesion causing mucopolysaccharidosis type I in cats;He;Mol. Genet. Metab.,1999

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