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| White matter disorders and cerebral calcification - narrow panel v0.11 | PEX19 |
Ellen McDonagh gene: PEX19 was added gene: PEX19 was added to White matter disorders and cerebral calcification - narrow panel. Sources: Expert Review Amber Mode of inheritance for gene: PEX19 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: PEX19 were set to Peroxisome biogenesis disorder 12A (Zellweger) |
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