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Pediatric cardiomyopathy: importance of genetic and metabolic evaluation
BACKGROUND: Cardiomyopathy is a heterogeneous disease with a strong genetic component. A research-based pediatric cardiomyopathy registry (PCMR) identified familial, syndromic, or metabolic causes in 30% of children. However, these results pre-dated clinical genetic testing. METHODS AND RESULTS: We...
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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3345128/ https://ncbi.nlm.nih.gov/pubmed/22555271 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.cardfail.2012.01.017 |
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