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Forum: Myotonia Congenita Forum
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Diagnosis Report

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?

Country: USA

Re: Diagnosis Report - by Jan (moderator) - Oct 20, 2014 9:21am
Re: Diagnosis Report - by Evgeniy - Oct 25, 2014 11:08am
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