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BabyScreen+ newborn screening v1.114 | KCNJ8 | Tommy Li Added phenotypes Sudden infant death syndrom for gene: KCNJ8 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
BabyScreen+ newborn screening v0.0 | KCNJ8 |
Zornitza Stark gene: KCNJ8 was added gene: KCNJ8 was added to gNBS. Sources: Expert Review Red,BabySeq Category C gene Mode of inheritance for gene: KCNJ8 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Phenotypes for gene: KCNJ8 were set to Sudden infant death syndrom |