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| Genomic newborn screening: BabyScreen+ v2.0 | UQCRB | Gene migrated from ENSG00000156467 to ENSG00000156467 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genomic newborn screening: BabyScreen+ v0.0 | UQCRB |
Zornitza Stark gene: UQCRB was added gene: UQCRB was added to gNBS. Sources: Expert Review Red,BabySeq Category C gene Mode of inheritance for gene: UQCRB was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: UQCRB were set to Mitochondrial complex III deficiency |
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