Associated Papers
Bi-allelic mutations in EGR2 cause autosomal recessive demyelinating neuropathy by disrupting the EGR2-NAB complex.
Lupo V et al.
European Journal of Neurology, 2020
Congenital hypomyelinating neuropathy with lethal conduction failure in mice carrying the Egr2 I268N mutation.
Baloh RH et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience, 2009
Molecular mechanisms of inherited demyelinating neuropathies.
Scherer SS et al.
Glia, 2008
Disruption of Krox20-Nab interaction in the mouse leads to peripheral neuropathy with biphasic evolution.
Desmazières A et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience, 2008
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