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)
Indexing
Wos®
Scopus®
Crossref®
Pubmed®
Google Scholar®
Publication Identifiers
Pubmed: 20937381
Scopus: 2-s2.0-78650281988
Wos: WOS:000285321500012
Source Identifiers
ISSN: 0925-4439
Export Publication Metadata
Marked List
 Add to Marked List
Info
At this moment we don't have any links to full text documens.

A place for researchers and their institutions

Useful Links

Get Help

© 2024 CRACS & Inesc TEC - All Rights Reserved Privacy Policy | Terms of Service