Ion‐ing out the genetic basis of peripheral neuropathy associated with agenesis of the corpus callosum: mutations in a cation transporter cause ACCPN

Name: Ion‐ing out the genetic basis of peripheral neuropathy associated with agenesis of the corpus callosum: mutations in a cation transporter cause ACCPN
Creator: R S Devon
Keywords: 0301 basic medicine, 0303 health sciences, 03 medical and health sciences

descriptionPublicationkeyboard_double_arrow_right Article 01 Jun 2003 English Publisher:WileyJournal:Clinical Genetics, volume 63, pages 456-457 (issn: 0009-9163, eissn: 1399-0004,

Authors: R S Devon;

doi: 10.1034/j.1399-0004.2003.00095.x

Ion‐ing out the genetic basis of peripheral neuropathy associated with agenesis of the corpus callosum: mutations in a cation transporter cause ACCPN

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Ion‐ing out the genetic basis of peripheral neuropathy associated with agenesis of the corpus callosum: mutations in a cation transporter cause ACCPN

Ion‐ing out the genetic basis of peripheral neuropathy associated with agenesis of the corpus callosum: mutations in a cation transporter cause ACCPN

3 Research products, page 1 of 1

The gene responsible for a severe form of peripheral neuropathy and agenesis of the corpus callosum maps to chromosome 15q.

Fine mapping the candidate region for peripheral neuropathy with or without agenesis of the corpus callosum in the French Canadian population

Deletion of KCC3 in parvalbumin neurons leads to locomotor deficit in a conditional mouse model of peripheral neuropathy associated with agenesis of the corpus callosum