Quote:
Originally Posted by kiwi33
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THank you Kiwi, i have just received my letter from Oxford.
SCN9a ,10a, 11a, trpa1 and NAGLU were all negative for known
channelopathies.
What do you think the chances are of them being able to find out the cause from the 100,000 genomes project? My neurologist said they still may not be able to identify it?
Thanks