Molecular heterogeneity in the infantile and juvenile forms of Sandhoff disease (O-variant GM2 gangliosidosis).-Reference-Cited by-同舟云学术

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Molecular heterogeneity in the infantile and juvenile forms of Sandhoff disease (O-variant GM2 gangliosidosis).

Published:1986-09 Issue:27 Volume:261 Page:12680-12685
ISSN:0021-9258
Container-title:Journal of Biological Chemistry
language:en
Short-container-title:Journal of Biological Chemistry

Author:

O'Dowd B F,Klavins M H,Willard H F,Gravel R,Lowden J A,Mahuran D J

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference42 articles.

1. Tay-Sachssche Krankheit mit Hexosaminidase-Defekt

2. Juvenile GM2 Gangliosidosis

3. A New Variant of Sandhoff's Disease

4. Adult (Chronic) GM2 Gangliosidosis

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3. Sandhoff Disease, Infantile, Juvenile, and Adult Form;Genetic Syndromes;2023

4. The dense-core plaques of Alzheimer’s disease are granulomas;Journal of Experimental Medicine;2022-06-22

5. Lysosomal gene Hexb displays haploinsufficiency in a knock-in mouse model of Alzheimer’s disease;IBRO Neuroscience Reports;2022-06

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