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| Genomic newborn screening: BabyScreen+ v2.1 | LPIN1 |
TRAIL SCHN gene: LPIN1 was added gene: LPIN1 was added to Genomic newborn screening: BabyScreen+. Sources: Expert Review Mode of inheritance for gene: LPIN1 was set to BIALLELIC, autosomal or pseudoautosomal Review for gene: LPIN1 was set to RED Added comment: Please tag as "TRAIL Study" Suggested by metabolic clinician. Known cause of severe rhabdomyolysis, early monitoring and treatment can improve outcomes. Sources: Expert Review |
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