Glb1 knockout mouse model shares natural history with type II GM1 gangliosidosis patients

Author:

Nicoli Elena-Raluca,Huebecker Mylene,Han Sangwoo T.,Garcia Karolyn,Munasinghe Jeeva,Lizak Martin,Latour Yvonne,Yoon Robin,Glase Brianna,Tyrlik Michal,Peiravi Morteza,Springer Danielle,Baker Eva H.,Priestman David,Sidhu Rohini,Kell Pamela,Jiang Xuntian,Kolstad Josephine,Kuhn Anna Luisa,Shazeeb Mohammed Salman,Acosta Maria T.,Proia Richard L.,Platt Frances M.,Tifft Cynthia J.

Funder

NIH

Publisher

Elsevier BV

Subject

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

Reference42 articles.

1. Generalized gangliosidosis: another inborn error of ganglioside metabolism?;O’Brien;Am J Dis Child,1965

2. β-Galactosidase Deficiency (β-Galactosidosis): GM1 Gangliosidosis and Morquio B Disease;Suzuki,2019

3. Lysosomal storage diseases;Platt;Nat Rev Dis Primers,2018

4. p-Galactosidase Deficiency (P-Galactosidosis): GM1 Gangliosidosis and Morquio B Disease Part 16: LYSOSOMAL DISORDERS. Cap 151;Suzuki,2011

5. The Metabolic and Molecular Bases of Inherited Disease;Fredrickson,1995

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