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Phenylketonuria as a protein misfolding disease: Mutant PG46S human phenylalanine hydroxylase has a propensity to self-associate and form amyloid fibrils

Authors :
Leandro, J.
Simonsen, N.
Almeida, Tavares
Paula Leandro
Flatmark, T.
Source :
ResearcherID, CIÊNCIAVITAE

Details

Database :
OpenAIRE
Journal :
ResearcherID, CIÊNCIAVITAE
Accession number :
edsair.dedup.wf.001..17d6664bd46c922e59a8e644bb21ef06

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