Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5892602 | Bone | 2009 | 8 Pages |
Abstract
Our study suggests that the novel G46X and C114Y mutations in exon 3 in WISP3 gene are responsible for PPD in Chinese patients. Furthermore, many heterozygous carriers (c.8004C>T and c.8209G>A) are found in the two families, suggesting the existence of a founder effect in the locality where they live, respectively.
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Authors
Hua Yue, Zhen-Lin Zhang, Jin-Wei He,