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| BabyScreen+ newborn screening v1.114 | FSCN2 | Tommy Li Added phenotypes Retinitis pigmentosa for gene: FSCN2 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| BabyScreen+ newborn screening v0.0 | FSCN2 |
Zornitza Stark gene: FSCN2 was added gene: FSCN2 was added to gNBS. Sources: Expert Review Red,BabySeq Category C gene Mode of inheritance for gene: FSCN2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Phenotypes for gene: FSCN2 were set to Retinitis pigmentosa |
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