A new lysozyme tyr54asn mutation causing amyloidosis in a family of Swedish ancestry with gastrointestinal symptoms
about
A Nanobody Binding to Non-Amyloidogenic Regions of the Protein Human Lysozyme Enhances Partial Unfolding but Inhibits Amyloid Fibril FormationA new family with hereditary lysozyme amyloidosis with gastritis and inflammatory bowel disease as prevailing symptoms.Serum Amyloid P Component Ameliorates Neurological Damage Caused by Expressing a Lysozyme Variant in the Central Nervous System of Drosophila melanogaster.The Significance of the Location of Mutations for the Native-State Dynamics of Human Lysozyme.Hereditary Lysozyme Amyloidosis Variant p.Leu102Ser Associates with Unique Phenotype.Hereditary lysozyme amyloidosis with sicca syndrome, digestive, arterial, and tracheobronchial involvement: case-based review.
P2860
A new lysozyme tyr54asn mutation causing amyloidosis in a family of Swedish ancestry with gastrointestinal symptoms
description
im September 2012 veröffentlichter wissenschaftlicher Artikel
@de
scientific article published on 14 September 2012
@en
wetenschappelijk artikel
@nl
наукова стаття, опублікована у вересні 2012
@uk
name
A new lysozyme tyr54asn mutati ...... with gastrointestinal symptoms
@en
A new lysozyme tyr54asn mutati ...... with gastrointestinal symptoms
@nl
type
label
A new lysozyme tyr54asn mutati ...... with gastrointestinal symptoms
@en
A new lysozyme tyr54asn mutati ...... with gastrointestinal symptoms
@nl
prefLabel
A new lysozyme tyr54asn mutati ...... with gastrointestinal symptoms
@en
A new lysozyme tyr54asn mutati ...... with gastrointestinal symptoms
@nl
P2093
P2860
P1433
P1476
A new lysozyme tyr54asn mutati ...... with gastrointestinal symptoms
@en
P2093
Brian Spencer
Carl O'Hara
Catherine Bartholomew
David C Seldin
Martha Skinner
Saulius Girnius
Tatiana Prokaeva
P2860
P304
P356
10.3109/13506129.2012.723074
P577
2012-09-14T00:00:00Z