Publication | Closed Access
Loss-of-function mutation of the AF9/MLLT3 gene in a girl with neuromotor development delay, cerebellar ataxia, and epilepsy
33
Citations
15
References
2005
Year
Developmental BiologyLoss-of-function MutationNeuromotor Development DelayGenetic DisorderMendelian DisorderGeneticsMolecular GeneticsGenetic FactorNeuroscienceAf9/mllt3 GeneDisease Gene IdentificationMedicineNeurogenetics
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