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"In the mouse, targeted deletion of the orthologous IC2 region results in growth restriction and loss of imprinting of six genes including Cdkn1c and Phlda2 when paternally inherited. xref By contrast, paternal transmission of 250–330 kb deletions, including most of the KCNQ1 gene, IC2 and KCNQ1OT1 is associated with normal phenotype in humans (refs. xref and xref ; also see xref )."