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Biallelic GTF2IRD1 variants in brothers with profound neurodevelopmental disorder: A possible novel disorder involving a critical gene for Williams syndrome |
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| Authors: | Christopher Thomas Cummings Lois Janelle Starr |
| Institution: | Department of Pediatrics, Children's Hospital and Medical Center, University of Nebraska Medical Center, Omaha, Nebraska, USA |
| Abstract: | |
| Keywords: | GTF2IRD1 neurodevelopmental disability Williams–Beuren syndrome |