The beta-glucuronidase intracisternal A particle insertion model results in similar overall MPSVII phenotype as the single base deletion model when on the same C57BL/6J mouse background

Author:

Devanney Sean C.,Gibney Joseph M.,Le Prell Colleen G.,Wronski Thomas J.,Aguirre J.I.,Mcdoom Issam,Heldermon Coy D.

Funder

NIH

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology

Reference26 articles.

1. Beta glucuronidase deficiency: report of clinical, radiologic, and biochemical features of a new mucopolysaccharidosis;Sly;J. Pediatr.,1973

2. Glycosaminoglycan storage disorders: a review;Coutinho;Biochem. Res. Int.,2012

3. Murine mucopolysaccharidosis type VII. Characterization of a mouse with beta-glucuronidase deficiency;Birkenmeier;J. Clin. Investig.,1989

4. Mucopolysaccharidosis type VII in a German shepherd dog;Silverstein Dombrowski;J. Am. Vet. Med. Assoc.,2004

5. Mutations and polymorphisms in GUSB gene in mucopolysaccharidosis VII (Sly Syndrome);Tomatsu;Hum. Mutat.,2009

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