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Re: No more free gen testing with the Periodic Paralysis Association?

Thanks a lot!

The simple testing for the most common mutations I have already done (at CeGaT, for a lot of money!). So it must be a full sequencing to detect deletions, duplications and splicing mutations in the intron.

I was once in a study for morbus pompe. They checked my pompe gen free of cost and found a new mutation, but heterozygot. So I don't have the pompe desease.

Studies are great! But I think that now noone else in the world has an interest in Myotonia.


Type of Myotonia: unknown

Country: Switzerland

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