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| Genomic newborn screening: BabyScreen+ v2.0 | ARL13B | Gene migrated from ENSG00000169379 to ENSG00000169379 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genomic newborn screening: BabyScreen+ v0.0 | ARL13B |
Zornitza Stark gene: ARL13B was added gene: ARL13B was added to gNBS. Sources: Expert Review Red,BabySeq Category C gene Mode of inheritance for gene: ARL13B was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: ARL13B were set to Joubert syndrome |
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