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Published in 2022 at "Frontiers in Genetics"
DOI: 10.3389/fgene.2022.1045738
Abstract: Mutations in CLN5 cause a subtype of neuronal ceroid lipofuscinosis (NCL) called CLN5 disease. The NCLs, commonly referred to as Batten disease, are a family of neurodegenerative lysosomal storage diseases that affect all ages and…
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Keywords:
cell;
cln5;
growth;
cln5 deficiency ... See more keywords