Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations.

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Published in Nat Genet on September 01, 2000

Authors

S E Hong1, Y Y Shugart, D T Huang, S A Shahwan, P E Grant, J O Hourihane, N D Martin, C A Walsh

Author Affiliations

1: Division of Neurogenetics, Department of Neurology, Beth Israel Deaconess Medical Center, Harvard Institutes of Medicine, Boston, Massachusetts, USA.

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