Now showing items 1-2 of 2

    • Byun, Nellie Eunjoo (2008-01-02)
      Department: Neuroscience
      Mutations in the human K-Cl cotransporter-3 (KCC3) gene lead to a severe neurological disorder called peripheral neuropathy associated with agenesis of the corpus callosum (ACCPN). At the same time as that discovery, the ...
    • Ding, Jinlong (2014-12-01)
      Department: Molecular Physiology and Biophysics
      Hereditary motor and sensory neuropathy associated with agenesis of the corpus callosum (HMSN/ACC or ACCPN) is an autosomal recessive disease caused by the disruption of the SLC12A6 gene, which encodes the K–Cl cotransporter-3 ...