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| BabyScreen+ newborn screening v1.114 | SCN1B | Tommy Li Added phenotypes Brugada syndrome for gene: SCN1B | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| BabyScreen+ newborn screening v0.0 | SCN1B |
Zornitza Stark gene: SCN1B was added gene: SCN1B was added to gNBS. Sources: Expert Review Red,BabySeq Category C gene Mode of inheritance for gene: SCN1B was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Phenotypes for gene: SCN1B were set to Brugada syndrome |
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