LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformation
Author:
Publisher
Oxford University Press (OUP)
Subject
Genetics(clinical),Genetics,Molecular Biology,General Medicine
Link
http://academic.oup.com/hmg/article-pdf/7/13/2029/1776308/7-13-2029.pdf
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