Phenylketonuria as a Protein Misfolding Disease: The Mutation Pg46S in Phenylalanine Hydroxylase Promotes Self-Association and Fibril Formation

AuthID
 P-002-Y38
5
Author(s)
Simonsen, N
·
Saraste, J
·
Flatmark, T
Document Type
Article
Year published
2011
Published
in BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, ISSN: 0925-4439
Volume: 1812, Issue: 1, Pages: 106-120 (15)
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Scopus®
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Publication Identifiers
Pubmed: 20937381
SCOPUS: 2-s2.0-78650281988
Wos: WOS:000285321500012
Source Identifiers
ISSN: 0925-4439
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