👤 Abraham Al-Ahmad

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An iPSC-Derived Neuron Model of CLN3 Disease Facilitates Small Molecule Phenotypic Screening.

Nihar Kinarivala, Ahmed Morsy, Ronak Patel +6 more · 2020 · ACS pharmacology & translational science · ACS Publications · added 2026-04-24
The neuronal ceroid lipofuscinoses (NCLs) are a family of rare lysosomal storage disorders. The most common form of NCL occurs in children harboring a mutation in the
no PDF DOI: 10.1021/acsptsci.0c00077
CLN3