Leandro, J.Simonsen, N.de Almeida, Tavares,Leandro, P.Flatmark, T.2015-12-302015-12-302008JOURNAL OF INHERITED METABOLIC DISEASE. - Vol. 31, Suppl. Suppl. 1 (AUG 2008), p. 3060141-8955http://hdl.handle.net/10451/21547application/pdfengEndocrinology & MetabolismGenetics & HeredityPhenylketonuria as a protein misfolding diseaseMutant PG46S human phenylalanine hydroxylase has a propensity to self-associate and form amyloid fibrilsjournal article