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| BabyScreen+ newborn screening v1.114 | PEX19 | Tommy Li Added phenotypes Zellweger syndrome for gene: PEX19 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| BabyScreen+ newborn screening v0.0 | PEX19 |
Zornitza Stark gene: PEX19 was added gene: PEX19 was added to gNBS. Sources: Expert Review Red,BabySeq Category C gene Mode of inheritance for gene: PEX19 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: PEX19 were set to Zellweger syndrome |
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