Functional analysis of novel DEAF1 variants identified through clinical exome sequencing expands DEAF1‐associated neurodevelopmental disorder (DAND) phenotype
Li Chen; Philip J. Jensik; Joseph T. Alaimo; Magdalena Walkiewicz; Seth Berger; Elizabeth Roeder; Eissa A. Faqeih; Jonathan A. Bernstein; Ann C. M. Smith; Sureni V. Mullegama; David W. Saffen; Sarah H. Elsea
Author Information: Department of Cellular and Genetic Medicine, School of Basic Medical Sciences
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