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...

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Main Authors: Hamidi Asl, Ladan, Liepnieks, Juris J., Hamidi Asl, Kamran, Uemichi, Tomoyuki, Moulin, Georges, Desjoyaux, Emmanuel, Loire, Robert, Delpech, Marc, Grateau, Gilles, Benson, Merrill D.
Format: Artigo
Sprog:Inglês
Udgivet: American Society for Investigative Pathology 1999
Fag:
Regular Articles
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC1853430/
https://ncbi.nlm.nih.gov/pubmed/9916936
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