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| Genomic newborn screening: BabyScreen+ v2.0 | GLUL | Gene migrated from ENSG00000135821 to ENSG00000135821 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Genomic newborn screening: BabyScreen+ v0.0 | GLUL |
Zornitza Stark gene: GLUL was added gene: GLUL was added to gNBS. Sources: Expert Review Red,BabySeq Category C gene Mode of inheritance for gene: GLUL was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: GLUL were set to Congenital brain dysgenesis due to glutamine synthetase deficiency |
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