Hereditary Amyloid Cardiomyopathy Caused by a Variant Apolipoprotein A1

Autosomal dominant hereditary amyloidosis with a unique cutaneous and cardiac presentation and death from heart failure by the sixth or seventh decade was found to be associated with a previously unreported point mutation (thymine to cytosine, nt 1389) in exon 4 of the apolipoprotein A1 (apoA1) gene...

Volledige beschrijving

Bewaard in:
Bibliografische gegevens
Hoofdauteurs: Hamidi Asl, Ladan, Liepnieks, Juris J., Hamidi Asl, Kamran, Uemichi, Tomoyuki, Moulin, Georges, Desjoyaux, Emmanuel, Loire, Robert, Delpech, Marc, Grateau, Gilles, Benson, Merrill D.
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: American Society for Investigative Pathology 1999
Onderwerpen:
Regular Articles
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC1853430/
https://ncbi.nlm.nih.gov/pubmed/9916936
Tags: Voeg label toe
Geen labels, Wees de eerste die dit record labelt!

Gelijkaardige items