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Frequency of and Consequences of Aortic Dilation in Noonan Syndrome
Noonan syndrome (NS) is a genetic disorder caused by mutations altering proteins relevant to RAS/mitogen-activated protein kinase (MAPK) signal transduction. Cardiac involvement is common, most prevalently pulmonary valve stenosis and hypertrophic cardiomyopathy. Since abnormal MAPK signaling contri...
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3947366/ https://ncbi.nlm.nih.gov/pubmed/24220280 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.amjcard.2013.09.034 |
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