https://www.selleckchem.com/pr....oducts/usp25-28-inhi
f the "GD suspects" with more developed algorithms and data-mining approaches is needed. This study was funded by Shire (now part of Takeda). This study was funded by Shire (now part of Takeda). Late infantile neuronal ceroid lipofuscinosis is an autosomal recessive disease caused by mutations in the CLN2/ gene, with secondary enzyme deficiency. In classical phenotypes, initial symptoms include seizures and delayed language development between 2 and 4years of age. This article describes the presentation of CLN2 disease in
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