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
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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
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Keywords
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Journal
BIOPOLYMERS
Volume -, Issue -, Pages -
Publisher
Wiley
Online
2020-02-29
DOI
10.1002/bip.23350
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