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Rare variant mutations identified in pediatric patients with dilated cardiomyopathy
Dilated cardiomyopathy (DCM) in infants and children can be partially explained by genetic cause but the catalogue of known genes is limited. We reviewed our database of 41 cases diagnosed with DCM before 18 years of age who underwent detailed clinical and genetic evaluation, and summarize here the...
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| Hauptverfasser: | , , , , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
2011
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3072577/ https://ncbi.nlm.nih.gov/pubmed/21483645 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ppedcard.2010.11.008 |
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