Amyloidogenicity and Clinical Phenotype Associated with Five Novel Mutations in Apolipoprotein A-I

The phenotype of hereditary apolipoprotein A-I amyloidosis is heterogeneous with some patients developing extensive visceral amyloid deposits and end-stage renal failure as young adults and others having only laryngeal and/or skin amyloid, which may be of little clinical consequence. Clinical manage...

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Bibliografische gegevens
Hoofdauteurs: Rowczenio, Dorota, Dogan, Ahmet, Theis, Jason D., Vrana, Julie A., Lachmann, Helen J., Wechalekar, Ashutosh D., Gilbertson, Janet A., Hunt, Toby, Gibbs, Simon D.J., Sattianayagam, Prayman T., Pinney, Jenny H., Hawkins, Philip N., Gillmore, Julian D.
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: American Society for Investigative Pathology 2011
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Regular Article
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3181365/
https://ncbi.nlm.nih.gov/pubmed/21820994
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajpath.2011.06.024
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