Publication | Open Access
Recurrent and founder mutations in the Netherlands: mutation p.K217del in troponin T2, causing dilated cardiomyopathy
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Citations
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References
2010
Year
CardiomyopathyGenetic DisorderGeneticsGenetic EpidemiologyPathologyMolecular GeneticsMutation P.k217delTroponin T2MedicineCardiologyFounder MutationsCardiovascular GeneticsCardiac Pathology
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