Skip to Main Content

Paper Details

Functional, histopathologic and natural history study of neuropathy associated with EGR2 mutations.
Neurogenetics
36
2007
Charcot-Marie-Tooth disease, EGR2, EGR2 gene, EGR2 mutations, I268N, NAB repressor binding site, R359W, cranial nerve dysfunction, inherited peripheral neuropathies, neuropathy, patients, respiratory compromise, zinc

Datasets

Release 1.2