Variant lysozyme C fibril [extracellular region]

Stable Identifier
R-HSA-976860
Type
Polymer
Species
Homo sapiens
Compartment
Locations in the PathwayBrowser
Literature References
PubMed ID Title Journal Year
8464497 Human lysozyme gene mutations cause hereditary systemic amyloidosis

Pepys, MB, Hawkins, PN, Booth, DR, Vigushin, DM, Tennent, GA, Soutar, AK, Totty, N, Nguyen, O, Blake, CC, Terry, CJ

Nature 1993
Participants
Participant Of