IndraLab

Statements

SCN5A binds ATXN3. 3 / 3
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"Brugada syndrome is a life-threatening, inherited arrhythmia disorder associated with autosomal dominant mutations in SCN5A [ xref - xref ], the gene encoding the human cardiac Na + channel α subunit (Nav1.5) [ xref ], which contains four homologous domains, each composed of six membrane-spanning segments, linked by cytoplasmic linkers."
19706159
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"Brugada syndrome (BrS) is a life-threatening, inherited arrhythmogenic syndrome associated with autosomal dominant mutations in SCN5A , the gene encoding the cardiac Na + channel alpha subunit (Na v 1.5)."
23308164
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"Brugada syndrome is a life-threatening, inherited arrhythmia disorder associated with autosomal dominant mutations in SCN5A, the gene encoding the human cardiac Na + channel α subunit (Nav1.5)."
19706159