DYRK1B haploinsufficiency in a family with metabolic syndrome and abnormal cognition. Issue 2 (16th November 2021)

• Record Type: Journal Article
• Authors: Orenstein, Naama; Gofin, Yoel; Shomron, Noam; Ruhrman‐Shahar, Noa; Magal, Nurit; Hagari, Ofir; Azulay, Noy; Bazak, Lily; Goldberg, Yael; Basel‐Salmon, Lina
• Is Part Of: Clinical genetics. Volume 101:Issue 2(2022)
• Page Start: 265
• Page End: 266
• Publication Date: 2021-11-16
• Subjects: Medical genetics -- Periodicals; 616.0420
• DOI: 10.1111/cge.14084
• Languages: English
• ISSNs: 0009-9163

Abstract

Abstract : A family with DYRK1B LOF variant offering to expand the phenotype beyond the metabolic syndrome.