https://colforsin.com/index.ph....p/internal-lipid-use
We conducted genome sequencing to search for unusual variation contributing to early-onset Alzheimer's disease condition (EOAD) and frontotemporal dementia (FTD). Discovery analysis ended up being performed on 435 cases and 671 settings of European ancestry. Burden screening for unusual difference associated with disease had been performed using filters predicated on variant rareness (less than one out of 10,000 or personal), computational forecast of deleteriousness (CADD) (10 or 15 thresholds
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