Browsing by Subject "Andermann Syndrome"
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(2014-12-01)Department: Molecular Physiology and BiophysicsHereditary 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 ...