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Deletions of NRXN1 (neurexin-1) predispose to a wide spectrum of developmental disorders
scientific article
Author/s
author: Eric M. Morrow, Shafali S Jeste, Gerard Berry, James F. Gusella, Christopher A. Walsh, David T. Miller, Leonard Rappaport, Children's Hospital Boston Genotype Phenotype Study Group
Work details
Publication date
June 1, 2010
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Language
English
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