SERKAL Syndrome: An Autosomal-Recessive Disorder Caused by a Loss-of-Function Mutation in WNT4
- 1 January 2008
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 82 (1), 39-47
- https://doi.org/10.1016/j.ajhg.2007.08.005
Abstract
No abstract availableKeywords
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