Abnormal Lipopigments and Lysosomal Residual Bodies in Metachromatic Leukodystrophy
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Publisher
Springer US
Link
http://link.springer.com/content/pdf/10.1007/978-1-4899-5339-1_21
Reference21 articles.
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3. Carpenter, S., 1982, Type 2 GM gangliosidosis and neuronal ceroid lipofuscinosis. Neurology 32: 575–576
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1. SCA34 caused by ELOVL4 L168F mutation is a lysosomal lipid storage disease sharing pathology features with neuronal ceroid lipofuscinosis and peroxisomal disorders;Acta Neuropathologica;2023-05-15
2. References;Metabolic and Degenerative Diseases of the Central Nervous System;1995
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