Phenylketonuria as a protein misfolding disease: The mutation pG46S in phenylalanine hydroxylase promotes self-association and fibril formation

Published 2010 View Full Article

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Title
Phenylketonuria as a protein misfolding disease: The mutation pG46S in phenylalanine hydroxylase promotes self-association and fibril formation
Authors
Keywords
-
Journal
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE
Volume 1812, Issue 1, Pages 106-120
Publisher
Elsevier BV
Online
2010-10-11
DOI
10.1016/j.bbadis.2010.09.015

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