Panel | Mode of inheritance | Details |
---|---|---|
1 panel | ||
Green in Skeletal muscle channelopathyR-numbers: R76 Signed-off version 3.0 | BOTH monoallelic and biallelic, autosomal or pseudoautosomal | Phenotypes Myotonia congenita, dominant OMIM:160800, Myotonia congenita, recessive OMIM:255700 |