doublecortin, a Brain-Specific Gene Mutated in Human X-Linked Lissencephaly and Double Cortex Syndrome, Encodes a Putative Signaling Protein

作者：Joseph G. Gleeson, Kristina M. Allen, Jeremy W. Fox, Edward D. Lamperti, Samuel Frank Berkovic, Ingrid Eileen Scheffer, Edward C. Cooper, William B. Dobyns, Sharon Minnerath, Margaret Elizabeth Ross, Christopher A. Walsh · 发表于：Cell · 年份：1998 · DOI：10.1016/s0092-8674(00)80899-5 · 被引用次数：1097 · 研究领域：Genetics and Neurodevelopmental Disorders、MicroRNA in disease regulation、Congenital heart defects research