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Literature for DOID 0050451: Brugada syndrome
Xenbase Articles
![Publications associated with this Disease Ontology entry or its descendants](img/icons/info1.png)
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Novel mechanism for Brugada syndrome: defective surface localization of an SCN5A mutant (R1432G)., Baroudi G,Pouliot V,Denjoy I,Guicheney P,Shrier A,Chahine M, Circ Res. June 22, 2001; 88(12):1524-4571. |
Conservation and divergence of protein pathways in the vertebrate heart.,
Federspiel JD,Tandon P,Wilczewski CM,Wasson L,Herring LE,Venkatesh SS,Cristea IM,Conlon FL,
PLoS Biol. September 6, 2019; 17(9):1545-7885.
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Identification of SCN5a p.C335R Variant in a Large Family with Dilated Cardiomyopathy and Conduction Disease.,
Sedaghat-Hamedani F,Rebs S,El-Battrawy I,Chasan S,Krause T,Haas J,Zhong R,Liao Z,Xu Q,Zhou X,Zhou X,Akin I,Zitron E,Frey N,Streckfuss-Bömeke K,Kayvanpour E,
Int J Mol Sci. November 30, 2021; 22(23):1422-0067.
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Functional cross-talk between phosphorylation and disease-causing mutations in the cardiac sodium channel Nav1.5.,
Galleano I,Harms H,Choudhury K,Khoo K,Delemotte L,Pless SA,
Proc Natl Acad Sci U S A. August 17, 2021; 118(33):1091-6490.
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