Recurrent and founder mutations in the Netherlands: cardiac Troponin I (TNNI3) gene mutations as a cause of severe forms of hypertrophic and restrictive cardiomyopathy (Q35129942)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Recurrent and founder mutations in the Netherlands: cardiac Troponin I (TNNI3) gene mutations as a cause of severe forms of hypertrophic and restrictive cardiomyopathy |
scientific article |
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Recurrent and founder mutations in the Netherlands: cardiac Troponin I (TNNI3) gene mutations as a cause of severe forms of hypertrophic and restrictive cardiomyopathy (English)
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A van den Wijngaard
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P Volders
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J P Van Tintelen
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J D H Jongbloed
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M P van den Berg
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R H Lekanne Deprez
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M M A M Mannens
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N Hofmann
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M Slegtenhorst
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D Dooijes
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M Michels
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Y Arens
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R Jongbloed
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B J M Smeets
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1 August 2011
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19
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7-8
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344-351
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