Isolated Lissencephaly Sequence and Double-Cortex Syndrome in a German Family with a Novel Doublecortin Mutation
Author:
Publisher
Georg Thieme Verlag KG
Subject
Clinical Neurology,General Medicine,Pediatrics, Perinatology, and Child Health
Link
http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-2000-7452.pdf
Cited by 13 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
1. X-linked intellectual disability gene CASK regulates postnatal brain growth in a non-cell autonomous manner;Acta Neuropathologica Communications;2016-03-31
2. New insights into genotype–phenotype correlations for the doublecortin-related lissencephaly spectrum;Brain;2013-01-01
3. Phenotypic and molecular characterization of a novelDCXdeletion and a review of the literature;Clinical Genetics;2009-08
4. The location of DCX mutations predicts malformation severity in X-linked lissencephaly;Neurogenetics;2008-08-07
5. Interfering with the brain: Use of RNA interference for understanding the pathophysiology of psychiatric and neurological disorders;Pharmacology & Therapeutics;2006-03
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