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PDF Availablehttps://doi.org/10.1136/jmedgenet-2015-103476
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Cite Journal: Journal of Medical Genetics |  Publication Date: Dec 15, 2015 |
 Citations: 43 |
Affiliation: University of California, Los Angeles, Alfaisal University, King Faisal Specialist Hospital & Research Centre, University of Washington, Children's Minnesota, University of Minnesota, California State University, Fresno, University of California, San Francisco, University of Hong Kong, Memorial University of Newfoundland
Autosomal recessively inherited mutations in WNT1 were recently identified as a cause of severe osteogenesis imperfecta (OI).1–6 This finding does not address the critical role of Wnt1 in mid-hindbrain development...
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