Publication | Open Access
Rare and de novo variants in 827 congenital diaphragmatic hernia probands implicate LONP1 as candidate risk gene
42
Citations
79
References
2021
Year
Candidate Risk GeneAllelic VariantDevelopmental BiologyGenetic DisorderGeneticsMolecular GeneticsMedical GeneticsDisease Gene IdentificationGenomicsMedicineGenetic MedicineVariant InterpretationClinical Genetics
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