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Netherlands Heart Journal
Gepubliceerd in:

01-05-2010 | Review article

Founder mutations in hypertrophic cardiomyopathy patients in the Netherlands

Auteurs: I. Christiaans*, E. A. Nannenberg*, D. Dooijes, R. J. E. Jongbloed, M. Michels, P. G. Postema, D. Majoor-Krakauer, A. van den Wijngaard, M. M. A. M. Mannens, J. P. van Tintelen, I. M. van Langen, A. A. M. Wilde

Gepubliceerd in: Netherlands Heart Journal | Uitgave 5/2010

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Extract

Hypertrophic cardiomyopathy (HCM) is a common genetic disease affecting at least one in 500 persons in the general population. In 1958 Teare gave a description of HCM when he reported a series of eight young patients who died suddenly from a disorder of the heart muscle.3,4 He was the first to describe the asymmetrical appearance of hypertrophy and its familial nature. He also described a disordered arrangement of muscle fibres at microscopic examination of the hearts of his cases, now known as myocyte disarray. …
vorige artikel Age is an independent risk factor for left atrial dysfunction: results from an observational study
volgende artikel The effect of insulin on the heart
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Metagegevens
Titel
Founder mutations in hypertrophic cardiomyopathy patients in the Netherlands
Auteurs
I. Christiaans*
E. A. Nannenberg*
D. Dooijes
R. J. E. Jongbloed
M. Michels
P. G. Postema
D. Majoor-Krakauer
A. van den Wijngaard
M. M. A. M. Mannens
J. P. van Tintelen
I. M. van Langen
A. A. M. Wilde
Publicatiedatum
01-05-2010
Uitgeverij
Bohn Stafleu van Loghum
Gepubliceerd in
Netherlands Heart Journal / Uitgave 5/2010
Print ISSN: 1568-5888
Elektronisch ISSN: 1876-6250
DOI
https://doi.org/10.1007/BF03091771

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