Quote:
Originally Posted by Kitt
There are mutations in the MFN2 gene that cause the most frequent form of autosomal dominant axonal form of Charcot-Marie-Tooth Disease. CMT2A.
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Hi Kitt,
I may have ask you this before but did you have testing done by a geneticist? I'm thinking if that is how you were diagnosed that way I might give it a try.
Thanks for the info. I appreciate it!
