Clinical manifestations in hereditary amyloidosis with the variant Glu54Gln transthyretin: a comment
Amyloid
.
2020 Jun;27(2):144.
doi: 10.1080/13506129.2019.1710126.
Epub 2020 Jan 6.
Authors
Ana Roteta Unceta Barrenechea
1
,
Miguel Ángel Aibar Arregui
2
,
Alejandro Andrés Gracia
1
,
Jorge Melero Polo
2
,
Carmen Lahuerta Pueyo
3
,
Sebastián Menao Guillén
3
,
Miguel Ángel Torralba Cabeza
4
Affiliations
1
Department of Nuclear Medicine, Hospital Clínico Universitario de Zaragoza (HCUZ), Aragón, Spain.
2
Department of Cardiology, Hospital Clínico Universitario de Zaragoza (HCUZ), Aragon, Spain.
3
Department of Clinical Biochemistry, Hospital Clínico Universitario de Zaragoza (HCUZ), Aragon, Spain.
4
Department of Internal Medicine, Hospital Clínico Universitario de Zaragoza (HCUZ), Aragon, Spain.
PMID:
31906714
DOI:
10.1080/13506129.2019.1710126
No abstract available
Publication types
Letter
Comment
MeSH terms
Amyloid Neuropathies, Familial*
Amyloidosis, Familial*
Humans
Prealbumin
Substances
Prealbumin