Genetics
Fatal familial insomnia results from inheriting a prion protein gene, on chromosome 20, with two characteristics:
- the pathogenic mutation D178N
- methionine at the polymorphic position 129
Related pages
Create an account to add page annotations
Add information to this page that would be handy to have on hand during a consultation, such as a web address or phone number. This information will always be displayed when you visit this page