Chatting with Katie tonight as she’s doing an English paper how we found Dr N and Mito disfunction came up.
Amazing, if you think about what we know now.
Now we know that mito isn’t the primary condition. In our case it is secondary to a genetic condition not previously associated with mitochondrial disfunction. That everything is a symptom of a genetic condition that we are working on identifying.
With us it’s most likely the kif1a gene, as Hugh and I carry similar recessive mutations on chromosome 2.
So amazing how far we’ve come within Dannys lifetime.
I can’t wait to see how much farther science goes.