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Short QT syndrome v1.4 | SCN3B | James Eden reviewed gene: SCN3B: Rating: RED; Mode of pathogenicity: ; Publications: 19862833, 30420954, 16301704; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown; Current diagnostic: yes | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Short QT syndrome v1.3 | SCN3B |
Ellen McDonagh Source North West GLH was added to SCN3B. Publications for gene SCN3B were changed from to 30420954; 19862833; 16301704 |
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Short QT syndrome v0.2 | SCN3B |
Sarah Leigh gene: SCN3B was added gene: SCN3B was added to Short QT syndrome. Sources: Brugada syndrome (Version 1.7) Mode of inheritance for gene: SCN3B was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown |