Associated Papers
A de novo CSDE1 variant causing neurodevelopmental delay, intellectual disability, neurologic and psychiatric symptoms in a child of consanguineous parents.
Gangfuß A et al.
American Journal of Medical Genetics. Part A, 2022
Wnt/β-catenin pathway and cell adhesion deregulation in CSDE1-related intellectual disability and autism spectrum disorders.
El Khouri E et al.
Molecular Psychiatry, 2021
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