Brugada Syndrome 7 (BRGDA7)

Brugada Syndrome 7(来自ICD-11)

别称:

Atrial Fibrillation, Familial, 16

Brgda7

Brugada Syndrome, Type 7

Atfb16

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Brugada Syndrome 7, is also known as atrial fibrillation, familial, 16. An important gene associated with Brugada Syndrome 7 is SCN3B (Sodium Voltage-Gated Channel Beta Subunit 3). Affiliated tissues include heart and heart-ventricle, and related phenotypes are permanent atrial fibrillation and paroxysmal atrial fibrillation

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