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| Additional findings_Paediatric v0.2 | GFM1 | Zornitza Stark Added phenotypes Combined oxidative phosphorylation deficiency 1 for gene: GFM1 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Additional findings_Paediatric v0.0 | GFM1 |
Zornitza Stark gene: GFM1 was added gene: GFM1 was added to Newborn Screening_BabySeq. Sources: Expert Review Green,BabySeq Category A gene Mode of inheritance for gene: GFM1 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: GFM1 were set to Combined oxidative phosphorylation deficiency 1 |
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