Associated Papers
Dominant Action of CLCN4 Neurodevelopmental Disease Variants in Heteromeric Endosomal ClC-3/ClC-4 Transporters.
Tettey-Matey A et al.
Cells, 2025
Genotype-phenotype correlation in CLCN4-related developmental and epileptic encephalopathy.
Sahly AN et al.
Human Genetics, 2024
Functional and clinical studies reveal pathophysiological complexity of CLCN4-related neurodevelopmental condition.
Palmer EE et al.
Molecular Psychiatry, 2023
Novel variants in the CLCN4 gene associated with syndromic X-linked intellectual disability.
Li S et al.
Frontiers in Neurology, 2023
37789889 (PubMed )
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