Neurology

Presence of val30Met and val122ile mutations in a patient with hereditary amyloidosis




Presence of val30Met and val122ile mutations in a patient with hereditary amyloidosis

Source link






Related posts

Don’t Label Me: I Am Not My Mental Illness

Newsemia

Combining hippocampal volume metrics to better understand Alzheimer’s disease progression in at-risk individuals

Newsemia

Early outcomes in youth with psychogenic nonsyncopal collapse

Newsemia

This website uses cookies to improve your experience. We'll assume you're ok with this, but you can opt-out if you wish. Accept Read More

Privacy & Cookies Policy