View in EDS

Oculoleptomeningeal Amyloidosis Secondary to the Rare Transthyretin c.381T>G (p.Ile127Met) Mutation.

Saved in:
Bibliographic Details
Title: Oculoleptomeningeal Amyloidosis Secondary to the Rare Transthyretin c.381T>G (p.Ile127Met) Mutation.
Authors: Mathieu, Francois1, Morgan, Erin2, So, Joyce3,4, Munoz, David G.4,5, Mason, Warren6, Kongkham, Paul1 paul.kongkham@uhn.ca
Source: World Neurosurgery. Mar2018, Vol. 111, p190-193. 4p.
Database: Academic Search Ultimate
Be the first to leave a comment!
You must be logged in first