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Recurrent and founder mutations in the Netherlands: mutation p.K217del in troponin T2, causing dilated cardiomyopathy
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Recurrent and founder mutations in the Netherlands: mutation p.K217del in troponin T2, causing dilated cardiomyopathy

Netherlands heart journal, 2010-10, Vol.18 (10), p.478-485

Bohn Stafleu van Loghum 2010 ;ISSN: 1568-5888 ;EISSN: 1876-6250 ;DOI: 10.1007/BF03091819 ;PMID: 20978592

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