reference/18755091

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bibliographicCitation	Leandro J, Simonsen N, Saraste J, Leandro P, Flatmark T. Phenylketonuria as a protein misfolding disease: The mutation pG46S in phenylalanine hydroxylase promotes self-association and fibril formation. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 2011 Jan;1812(1):106–20. doi: 10.1016/j.bbadis.2010.09.015.
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date	201101
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language	English
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title	Phenylketonuria as a protein misfolding disease: The mutation pG46S in phenylalanine hydroxylase promotes self-association and fibril formation
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