QuickView for CLCN4;jsessionid=1D3808DCBF141C79D79BD845E60F893A (gene)

1. Analysis of CLCN4 gene variant in a child with Raynaud-Claes syndrome].
2. Developmental and epileptic encephalopathy in a young Italian woman with a de novo missense variant …
3. Functional Characterization of CLCN4 Variants Associated With X-Linked Intellectual Disability and E…
4. Novel CLCN4 variant associated with syndromic X-linked intellectual disability in a Chinese girl: a …
5. Clcn4-2 genomic structure differs between the X locus in Mus spretus and the autosomal locus in Mus …

There were no clinical trials for CLCN4;jsessionid=1D3808DCBF141C79D79BD845E60F893A