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Re: Diagnosis Report

Quote: Leroy
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.


Hello. Tell your family was sick?

Type of Myotonia: Bekkera

Country: Russia

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