Associated Papers
CERT1 mutations perturb human development by disrupting sphingolipid homeostasis.
Gehin C et al.
The Journal of Clinical Investigation, 2023
Intellectual-disability-associated mutations in the ceramide transport protein gene CERT1 lead to aberrant function and subcellular distribution.
Tamura N et al.
The Journal of Biological Chemistry, 2021
Intellectual disability-associated gain-of-function mutations in CERT1 that encodes the ceramide transport protein CERT.
Murakami H et al.
Plos One, 2020
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