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![OMIM Entry - # 230500 - GM1-GANGLIOSIDOSIS, TYPE I](https://www.iarticlesnet.com/pub/img/site/s_42.jpeg)
OMIM Entry - # 230500 - GM1-GANGLIOSIDOSIS, TYPE I
瀏覽:1066
日期:2024-09-06
GM1-Gangliosidosis is an autosomal recessive lysosomal storage disease
characterized by accumulation of ganglioside substrates in lysosomes. Clinically
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