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| Short QT syndrome v1.4 | SCN4B | James Eden reviewed gene: SCN4B: 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 | SCN4B |
Ellen McDonagh Source North West GLH was added to SCN4B. Publications for gene SCN4B were changed from to 30420954; 19862833; 16301704 |
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| Short QT syndrome v0.2 | SCN4B |
Sarah Leigh gene: SCN4B was added gene: SCN4B was added to Short QT syndrome. Sources: Long QT syndrome (Version 1.5),Emory Genetics Laboratory Mode of inheritance for gene: SCN4B was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown |
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