Phenylketonuria as a protein misfolding disease: The mutation pG46S in phenylalanine hydroxylase promotes self-association and fibril formation.
- DOI
- 10.1016/j.bbadis.2010.09.015
- Published
- 2011 Jan
- Container
- Biochimica et biophysica acta
- Publisher
- Not recorded
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1016/j.bbadis.2010.09.015,
title = {Phenylketonuria as a protein misfolding disease: The mutation pG46S in phenylalanine hydroxylase promotes self-association and fibril formation.},
author = {Leandro J and Simonsen N and Saraste J and Leandro P and Flatmark T},
year = {2011},
journal = {Biochimica et biophysica acta},
doi = {10.1016/j.bbadis.2010.09.015},
url = {https://doi.org/10.1016/j.bbadis.2010.09.015}
}RIS
TY - JOUR TI - Phenylketonuria as a protein misfolding disease: The mutation pG46S in phenylalanine hydroxylase promotes self-association and fibril formation. AU - Leandro J AU - Simonsen N AU - Saraste J AU - Leandro P AU - Flatmark T PY - 2011 JO - Biochimica et biophysica acta DO - 10.1016/j.bbadis.2010.09.015 UR - https://doi.org/10.1016/j.bbadis.2010.09.015 ER -
APA
J, L., N, S., J, S., P, L., & T, F. (2011). Phenylketonuria as a protein misfolding disease: The mutation pG46S in phenylalanine hydroxylase promotes self-association and fibril formation.. Biochimica et biophysica acta. https://doi.org/10.1016/j.bbadis.2010.09.015
Source records
- pubmed · retrieved 2026-11-10T12:57:00.680Z