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Improved access to life insurance after genetic diagnosis of familial hypercholesterolaemia: cross-sectional postal questionnaire study

A decade ago, in the initial stage of genetic testing for familial hypercholesterolaemia (FH) in The Netherlands, it was reported that such screening decreased access to affordable life insurance for mutation carriers. In 2003, in order to improve access to insurance for FH mutation carriers, insure...

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Detalhes bibliográficos
Main Authors: Huijgen, Roeland, Homsma, Sietske JM, Hutten, Barbara A, Kindt, Iris, Vissers, Maud N, Kastelein, John JP, van Rijckevorsel, Jan LA
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group 2012
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3376271/
https://ncbi.nlm.nih.gov/pubmed/22293687
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2012.5
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