| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 8624794 | Bone | 2018 | 6 Pages |
Abstract
The reported biallelic WNT1 variants cause loss of WNT1 function and lead to a severe bone fragility phenotype with conspicuous involvement of the spine.
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Authors
Yanqin Lu, Xiuzhi Ren, Yanzhou Wang, Ghalib Bardai, Marc Sturm, Yunzhang Dai, Olaf Riess, Yao Zhang, Hu Li, Tianyou Li, Naixiang Zhai, Jian Zhang, Frank Rauch, Jinxiang Han,