Publication | Open Access
De novo truncating variants in the intronless IRF2BPL are responsible for developmental epileptic encephalopathy
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Citations
11
References
2018
Year
Developmental BiologyIntronless Irf2bplDevelopmental Epileptic EncephalopathyGenetic DisorderGeneticsMolecular GeneticsNeuroscienceDisease Gene IdentificationMedicineVariant InterpretationNeurogenetics
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