Publication | Open Access
Loss of lysosomal association of cystatin B proteins representing progressive myoclonus epilepsy, EPM1, mutations
77
Citations
35
References
2004
Year
Molecular NeuroscienceMendelian DisorderGenetic DisorderProgressive Myoclonus EpilepsyGeneticsMolecular GeneticsCystatin BMedicineCell BiologyLysosomal Storage DiseaseNeurogeneticsLysosomal Association
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