Association of LMX1A Genetic Polymorphisms With Susceptibility to Congenital Scoliosis in Chinese Han Population-Reference-Cited by-同舟云学术

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Association of LMX1A Genetic Polymorphisms With Susceptibility to Congenital Scoliosis in Chinese Han Population

Published:2014-10 Issue:21 Volume:39 Page:1785-1791
ISSN:0362-2436
Container-title:Spine
language:en
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Author:

Wu Nan,Yuan Suomao,Liu Jiaqi,Chen Jun,Fei Qi,Liu Sen,Su Xinlin,Wang Shengru,Zhang Jianguo,Li Shugang,Wang Yipeng,Qiu Guixing,Wu Zhihong

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Clinical Neurology,Orthopedics and Sports Medicine

Reference27 articles.

1. Congenital Scoliosis Caused by a Unilateral Failure of Vertebral Segmentation With Contralateral Hemivertebrae

2. When body segmentation goes wrong

3. Congenital and Idiopathic Scoliosis: Clinical and Genetic Aspects

4. Vertebrate Segmentation: From Cyclic Gene Networks to Scoliosis

5. The mouse notches up another success: understanding the causes of human vertebral malformation

Cited by 7 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. A Missense Mutation in LMX1A in a Patient With Moebius Syndrome: A Case Report;Cureus;2022-10-10

2. High methylation of lysine acetyltransferase 6B is associated with the Cobb angle in patients with congenital scoliosis;Journal of Translational Medicine;2020-05-24

3. The diagnostic performance of serum LIM homeobox transcription factor 1 alpha in patients with gastric cancer;Medicine;2019-05

4. A comprehensive review of the diagnosis and management of congenital scoliosis;Child's Nervous System;2018-08-04

5. The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease;Human Genetics;2018-07

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