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The abnormal C-terminus caused by DVL1 variants impacts Robinow syndrome phenotypes.

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Bibliographic Details
Title:	The abnormal C-terminus caused by DVL1 variants impacts Robinow syndrome phenotypes.
Authors:	Tophkhane SS; Life Sciences Institute and Faculty of Dentistry, University of British Columbia, 2350 Health Sciences Mall Vancouver, BC, V6T 1Z3, Canada., Akarsu G; Department of Molecular Biology and Biochemistry, Centre for Cell Biology, Development and Disease, Simon Fraser University, 8888 University Drive, Burnaby, BC, V5A 1S6, Canada., Gignac SJ; Life Sciences Institute and Faculty of Dentistry, University of British Columbia, 2350 Health Sciences Mall Vancouver, BC, V6T 1Z3, Canada., Xie X; Life Sciences Institute and Faculty of Dentistry, University of British Columbia, 2350 Health Sciences Mall Vancouver, BC, V6T 1Z3, Canada., Fu K; Life Sciences Institute and Faculty of Dentistry, University of British Columbia, 2350 Health Sciences Mall Vancouver, BC, V6T 1Z3, Canada., Verheyen EM; Department of Molecular Biology and Biochemistry, Centre for Cell Biology, Development and Disease, Simon Fraser University, 8888 University Drive, Burnaby, BC, V5A 1S6, Canada., Richman JM; Life Sciences Institute and Faculty of Dentistry, University of British Columbia, 2350 Health Sciences Mall Vancouver, BC, V6T 1Z3, Canada.
Source:	Human molecular genetics [Hum Mol Genet] 2026 Jun 06; Vol. 35 (14).
Publication Type:	Journal Article
Journal Info:	Publisher: IRL Press at Oxford University Press Country of Publication: England NLM ID: 9208958 Publication Model: Print Cited Medium: Internet ISSN: 1460-2083 (Electronic) Linking ISSN: 09646906 NLM ISO Abbreviation: Hum Mol Genet Subsets: MEDLINE
Database:	MEDLINE Ultimate

Description
ISSN:	1460-2083
DOI:	10.1093/hmg/ddag053