# PITX2c Loss-of-Function Mutations Responsible for Congenital Atrial Septal Defects

**Type:** Papers  
**Canonical URL:** https://scholariq.org/papers/pitx2c-loss-of-function-mutations-responsible-for-congenital-atrial-septal/

## Facts

| Field | Value |
| --- | --- |
| Author Names | Fang Yuan,Lan Zhao,Juan Wang,Wei Zhang,Xin Li,Xing‐Biao Qiu,Ruogu Li,Ying‐Jia Xu,Lei Xu,Xing-Kai Qu,Weiyi Fang,Yi‐Qing Yang |
| Citations | 30 |
| DOI | 10.7150/ijms.6809 |
| Fields | Biochemistry, Genetics and Molecular Biology,Medicine,Neuroscience |
| Open Access | true |
| OA Status | gold |
| OA URL | https://www.medsci.org/v10p1422.pdf |
| OpenAlex ID | https://openalex.org/W2159538525 |
| PMID | 23983605 |
| Type | article |
| Year | 2013 |

## Paper authors

- [Xin Li](https://scholariq.org/researchers/xin-li/)

## Paper journal

- [International Journal of Medical Sciences](https://scholariq.org/journals/international-journal-of-medical-sciences/)

## Paper primary topic

- [Congenital heart defects research](https://scholariq.org/topics/congenital-heart-defects-research/)

## Paper topics

- [Congenital heart defects research](https://scholariq.org/topics/congenital-heart-defects-research/)
- [Congenital Heart Disease Studies](https://scholariq.org/topics/congenital-heart-disease-studies/)
- [Williams Syndrome Research](https://scholariq.org/topics/williams-syndrome-research/)

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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.