Genotype-phenotype correlations for EPM2A mutations in Lafora's progressive myoclonus epilepsy: exon 1 mutations associate with an early-onset cognitive deficit subphenotype.
暂无分享,去创建一个
M. T. Medina | K. Yamakawa | A. Delgado-Escueta | A. Rabinowicz | S. Ganesh | A. Rasmussen | Toshimitsu Suzuki | M. Alonso | J. Bailey | A. Ochoa | S. Bohlega | A. J. Prado | Alfredo E Thomson | C. Riggio | G. Avanzini | S. Francheschetti