A novel point mutation A170P in the SHOX gene defines impaired nuclear translocation as a molecular cause for Leri-Weill dyschondrosteosis and Langer dysplasia
- 1 June 2004
- journal article
- case report
- Published by BMJ in Journal of Medical Genetics
- Vol. 41 (6) , e83
- https://doi.org/10.1136/jmg.2003.016402
Abstract
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