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| Additional findings_Paediatric v1.0 | SCN1A | Gene migrated from ENSG00000144285 to ENSG00000144285 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Additional findings_Paediatric v0.2 | SCN1A |
Zornitza Stark gene: SCN1A was added gene: SCN1A was added to Newborn Screening_BabySeq. Sources: Expert Review Green,BabySeq Category A gene Mode of inheritance for gene: SCN1A was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: SCN1A were set to Dravet syndrome |
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