A double point mutation in the DNA-binding region of Egr2 switches its function from inhibition to induction of proliferation: A potential contribution to the development of congenital hypomyelinating neuropathy
Author:
Publisher
Elsevier BV
Subject
Neurology
Cited by 16 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
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3. A novel family with axonal Charcot‐Marie‐Tooth disease caused by a mutation in the EGR2 gene;Journal of the Peripheral Nervous System;2019-03-28
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