Phenylketonuria as a protein misfolding disease: The mutation pG46S in phenylalanine hydroxylase promotes self-association and fibril formation. (Q47837284)
Jump to navigation
Jump to search
scientific article published on 16 October 2010
Language | Label | Description | Also known as |
---|---|---|---|
English | Phenylketonuria as a protein misfolding disease: The mutation pG46S in phenylalanine hydroxylase promotes self-association and fibril formation. |
scientific article published on 16 October 2010 |
Statements
1 reference
Phenylketonuria as a protein misfolding disease: The mutation pG46S in phenylalanine hydroxylase promotes self-association and fibril formation. (English)
1 reference
Torgeir Flatmark
1 reference
João Leandro
1 reference
Nina Simonsen
1 reference
Jaakko Saraste
1 reference
Paula Leandro
1 reference
16 October 2010
1 reference
1 reference
1812
1 reference
1
1 reference
106-120
1 reference
Identifiers
1 reference
1 reference