GM1 gangliosidosis in shiba dogs

Author:

Yamato O.1,Masuoka Y.1,Tajima M.1,Omae S.1,Maede Y.1,Ochiai K.2,Hayashida E.2,Umemura T.2,Lijima M.3

Affiliation:

1. Laboratory of Internal Medicine; Hokkaido University; Sapporo 060-0818 Japan

2. Laboratory of Comparative Pathology, Department of Veterinary Clinical Sciences, Graduate School of Veterinary Medicine; Hokkaido University; Sapporo 060-0818 Japan

3. Pakira Animal Hospital; Ishikari 061-3201 Japan

Publisher

Wiley

Subject

General Veterinary,General Medicine

Reference31 articles.

1. Inherited lysosomal storage disease associated with deficiencies of β-galactosidase and α-neuraminidase in sheep;AHERN-RINDELL;American Journal of Medical Genetics,1988

2. Application of lectin histochemistry and carbohydrate analysis to the characterisation of lysosomal storage diseases;ALROY;Carbohydrate Research,1991

3. Canine GM1-gangliosidosis. A clinical, morphologic, histochemical and biochemical comparison of two different models;ALROY;American Journal of Pathology,1992

4. Neurovisceral and skeletal GM1 gangliosidosis in dogs with β-galactosidase deficiency;ALROY;Science,1985

5. Neuronal GM1 gangliosidosis in a Siamese cat with β-galactosidase deficiency;BAKER;Science,1971

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