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| BabyScreen+ newborn screening v1.114 | MYO1C | Tommy Li Added phenotypes Sensorineural hearing loss for gene: MYO1C | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| BabyScreen+ newborn screening v0.0 | MYO1C |
Zornitza Stark gene: MYO1C was added gene: MYO1C was added to gNBS. Sources: Expert Review Red,BabySeq Category C gene Mode of inheritance for gene: MYO1C was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: MYO1C were set to Sensorineural hearing loss |
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