Phenylketonuria as a Protein Misfolding Disease: Mutant Pg46S Human Phenylalanine Hydroxylase Has a Propensity to Self-Associate and Form Amyloid Fibrils

AuthID
 P-003-XDR
5
Author(s)
Simonsen, N
·
de Almeida, TI
·
Tipo de Documento
Abstract
Year published
2008
Publicado
in JOURNAL OF INHERITED METABOLIC DISEASE, ISSN: 0141-8955
Volume: 31, Páginas: 77-77 (1)
Indexing
Wos®
Publication Identifiers
Wos: WOS:000258656400306
Source Identifiers
ISSN: 0141-8955
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