# Gene mutation spectrum and genotype-phenotype correlation in a cohort of Chinese osteogenesis imperfecta patients revealed by targeted next generation sequencing

**Type:** Papers  
**Canonical URL:** https://scholariq.org/papers/gene-mutation-spectrum-and-genotype-phenotype-correlation-in-a-cohort-of-chinese/

## Facts

| Field | Value |
| --- | --- |
| Author Names | Y. Liu,Asan,Dexuan Ma,Fang Lv,Xin Xu,Jianwei Wang,Weibo Xia,Yan Jiang,O. Wang,Xiaoping Xing,W. Yu,Jin Wang,Junwei Sun,Lijie Song,Yu Zhu,Huanming Yang,Jin Wang,Ke Li |
| Citations | 80 |
| DOI | 10.1007/s00198-017-4143-8 |
| Fields | Biochemistry, Genetics and Molecular Biology |
| Open Access | false |
| OA Status | closed |
| OpenAlex ID | https://openalex.org/W4232875174 |
| PMID | 28725987 |
| Type | article |
| Year | 2017 |

## Paper authors

- [Xiaoping Xing](https://scholariq.org/researchers/xiaoping-xing/)
- [Yan Jiang](https://scholariq.org/researchers/yan-jiang/)

## Paper primary topic

- [Connective tissue disorders research](https://scholariq.org/topics/connective-tissue-disorders-research/)

## Paper topics

- [Connective tissue disorders research](https://scholariq.org/topics/connective-tissue-disorders-research/)
- [Dermatological and Skeletal Disorders](https://scholariq.org/topics/dermatological-and-skeletal-disorders/)
- [TGF-β signaling in diseases](https://scholariq.org/topics/tgf-signaling-in-diseases/)

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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.