The congenital cataract‐causing mutations P20R and A171T are associated with important changes in the amyloidogenic feature, structure and chaperone‐like activity of human αB‐crystallin

Title
The congenital cataract‐causing mutations P20R and A171T are associated with important changes in the amyloidogenic feature, structure and chaperone‐like activity of human αB‐crystallin
Authors
Keywords
-
Journal
BIOPOLYMERS
Volume -, Issue -, Pages -
Publisher
Wiley
Online
2020-02-29
DOI
10.1002/bip.23350

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