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| Additional findings_Paediatric v0.2 | SCN4A |
Zornitza Stark Source BabySeq Category C gene was added to SCN4A. Source Expert Review Red was added to SCN4A. Added phenotypes Hypokalemic periodic paralysis, type 2 for gene: SCN4A Rating Changed from Green List (high evidence) to Red List (low evidence) |
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| Additional findings_Paediatric v0.2 | SCN4A |
Zornitza Stark gene: SCN4A was added gene: SCN4A was added to Newborn Screening_BabySeq. Sources: Expert Review Green,BabySeq Category A gene Mode of inheritance for gene: SCN4A was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Phenotypes for gene: SCN4A were set to Hyperkalemic periodic paralysis, type 2 |
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