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One or more keywords matched the following properties of Familial amyloid cardiomyopathy due to TTR mutations: an underdiagnosed cause of restrictive cardiomyopathy [corrected].

PropertyValue
has major subject area list Amyloidosis; Cardiomyopathy, Restrictive; DNA; Genetic Predisposition to Disease; Mutation
information resource reference Ruberg FL, Judge DP, Maurer MS. Familial amyloid cardiomyopathy due to TTR mutations: an underdiagnosed cause of restrictive cardiomyopathy [corrected]. J Card Fail. 2009 Jun; 15(5):464. PMID: 19477408.
label Familial amyloid cardiomyopathy due to TTR mutations: an underdiagnosed cause of restrictive cardiomyopathy [corrected].

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  • Amyloid
  • Cardiomyopathy