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Exome Analysis of a Family with Wolff–Parkinson–White Syndrome Identifies a Novel Disease Locus
Wolff–Parkinson–White (WPW) syndrome is a common cause of supraventricular tachycardia that carries a risk of sudden cardiac death. To date, mutations in only one gene, PRKAG2, which encodes the 5’ -AMP-activated protein kinase subunit γ-2, have been identified as causative for WPW. DNA samples from...
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Publicado no: | Am J Med Genet A |
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Main Authors: | , , , , , , , , , , , , , , |
Formato: | Artigo |
Idioma: | Inglês |
Publicado em: |
2015
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Assuntos: | |
Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4896306/ https://ncbi.nlm.nih.gov/pubmed/26284702 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.a.37297 |
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