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Phenylketonuria as a protein misfolding disease: The mutation pG46S in phenylalanine hydroxylase promotes self-association and fibril formation.
Leandro, João; Simonsen, Nina; Saraste, Jaakko; Leandro, Paula; Flatmark, Torgeir.
Affiliation
  • Leandro J; Department of Biomedicine, University of Bergen, Jonas Lies vei 91, N-5009 Bergen, Norway.
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

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