QuickView for CLCN1;jsessionid=1D3808DCBF141C79D79BD845E60F893A (gene)

1. A complex CLCN1 variant associated with hereditary myotonia in a mixed-breed dog.
2. Hereditary myotonia in cats associated with a new homozygous missense variant p.Ala331Pro in the mus…
3. Functional and Structural Characterization of ClC-1 and Nav1.4 Channels Resulting from CLCN1 and SCN…
4. Coexistence of SCN4A and CLCN1 mutations in a family with atypical myotonic features: A clinical and…
5. A coupled enzyme assay for detection of selenium-binding protein 1 (SELENBP1) methanethiol oxidase (…

There were no clinical trials for CLCN1;jsessionid=1D3808DCBF141C79D79BD845E60F893A