AXIN1 bi-allelic variants disrupting the C-terminal DIX domain cause craniometadiaphyseal osteosclerosis with hip dysplasia
Authors:
- 14 August 2023
- journal article
- research article
- Published by Elsevier in The American Journal of Human Genetics
- Vol. 110 (9) , 1470-1481
Abstract
No abstract availableKeywords
Funding Information
- Deutsche Forschungsgemeinschaft
- Bundesministerium für Forschung, Technologie und Raumfahrt (031L0234A)
- Bundesministerium für Bildung Wissenschaft und Forschung
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