Single nucleotide polymorphisms of PCP pathway related genes participate in the occurrence and development of neural tube defect

Author:

Liu Yan12ORCID,Dong Liang3ORCID,Zhi Xiufang2ORCID,Liu Yang4ORCID,Zhao Linsheng5ORCID,Xu Xiaowei6ORCID,Wang Lu6ORCID,Zheng Jie2ORCID,Pu Linjie4ORCID,Gu Chunyu4ORCID,Shu Jianbo67ORCID,Cai Chunquan67ORCID

Affiliation:

1. Department of Nephrology Tianjin Children's Hospital (Children's Hospital of Tianjin University) Tianjin China

2. Graduate School Tianjin Medical University Tianjin China

3. Department of Pediatric General Surgery Tianjin Children's Hospital (Children’s Hospital of Tianjin University) Tianjin China

4. Department of Neonatology Tianjin Children's Hospital (Children’s Hospital of Tianjin University) Tianjin China

5. Department of Pathology Tianjin Children's Hospital (Children’s Hospital of Tianjin University) Tianjin China

6. Institute of Pediatrics Tianjin Children's Hospital (Children’s Hospital of Tianjin University) Tianjin China

7. Tianjin Key Laboratory of Birth Defects for Prevention and Treatment Tianjin China

Funder

National Natural Science Foundation of China

Tianjin Science and Technology Committee

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

Reference30 articles.

1. Cranial neural tube defect after trimethoprim exposure

2. Common dysregulation of Wnt/Frizzled receptor elements in human hepatocellular carcinoma

3. Genetic evidence in planar cell polarity signaling pathway in human neural tube defects

4. The association of VANGL1 gene polymorphisms and neural tube defects in Han population of northern China;Cai C. Q.;Chinese Journal of Pediatric Surgery,2013

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