Publication | Closed Access
Novel EXOSC9 variants cause pontocerebellar hypoplasia type 1D with spinal motor neuronopathy and cerebellar atrophy
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Citations
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References
2020
Year
Novel Exosc9 VariantsNeurodegenerative DiseasesCerebellar AtrophySpinal Cord InjuryNeurological DisorderGenetic DisorderGeneticsDegenerative DiseaseNeurologyNeuroscienceNeuropathologyMedicineSpinal MotorNeurogenetics
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