Phenylketonuria as a protein misfolding disease: The mutation pG46S in phenylalanine hydroxylase promotes self-association and fibril formation.
Biochim Biophys Acta
; 1812(1): 106-20, 2011 Jan.
Article
in En
| MEDLINE
| ID: mdl-20937381
Full text:
1
Database:
MEDLINE
Main subject:
Phenylalanine Hydroxylase
/
Protein Folding
/
Mutation
Type of study:
Prognostic_studies
/
Risk_factors_studies
Language:
En
Journal:
Biochim Biophys Acta
Year:
2011
Type:
Article
Affiliation country:
Norway