Jump to content

Recommended Posts

Posted
CJD is an example of a disease caused by the misfolding of the protein PrP©

I have been researching this disease somewhat and have discovered there are several variants including sporadic CJD and variant CJD.


It appears that the different variants of the disease have different risk factors and different physiological effects. Given that they are all caused by the misfolding of the same protein - PrP© - I was hoping someone could explain to me why the physiological effects of each variant differ in some respects [including:median age of death, duration of illness and some clinical signs/symptoms]


thanks

Create an account or sign in to comment

You need to be a member in order to leave a comment

Create an account

Sign up for a new account in our community. It's easy!

Register a new account

Sign in

Already have an account? Sign in here.

Sign In Now
×
×
  • Create New...

Important Information

We have placed cookies on your device to help make this website better. You can adjust your cookie settings, otherwise we'll assume you're okay to continue.