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...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Kindel, Steven J., Miller, Erin M., Gupta, Resmi, Cripe, Linda H., Hinton, Robert B., Spicer, Robert L., Towbin, Jeffrey A., Ware, Stephanie M.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: 2012
Gaiak:
Article
Sarrera elektronikoa: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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