This forum has been closed for comments. You can still search archived messages.
Visit the Non-Dystrophic Myotonias Facebook Group
DNA variant: Disease-associated mutation,heterozygous/ Inheritance : Unknown/ No abnormal DNA SCN4 gene/Analysis DNA identified two known disease-associated mutations in the CLCN1 gene tested causing mutations associated with Myotonia Congenita.
Type of Myotonia: M?